GeneBe
114genomic databases found
/ clinvar
Public DURING_UPLOAD

A Public Database of Genetic Variants

tmptable homo_sapiens VARIANT 0.0.2-20260928
Inspect
/ cosmic_genomescreensmutant_hg38
Public

COSMIC v104 GenomeScreensMutant GRCh38

tmptable homo_sapiens VARIANT 0.0.1-104
Inspect
/ cosmic_noncodingvariants_hg38
Public

COSMIC v104 NonCodingVariants GRCh38

tmptable homo_sapiens VARIANT 0.0.1-104
Inspect
/ schema
Public

SCHEMA schizophrenia case/control exome results

homo_sapiens GRCh38 VARIANT 0.0.2-20260812
Inspect
/ bipex
Public

BipEx bipolar disorder case/control exome results

homo_sapiens GRCh38 VARIANT 0.0.2-20220110
Inspect
/ epi25
Public

Epi25 epilepsy case/control exome results

homo_sapiens GRCh38 VARIANT 0.0.2-20230922
Inspect
/ korea4k
Public

Korea4K allele frequencies

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ china_map
Public

ChinaMAP Phase 1 allele frequencies

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ vesm_3b
Public

VESM-3B variant effect scores hg38

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ gpn-star-hg38-m447-200m
Public

GPN-Star (mammals, 200M) - genome-wide variant effect log-likelihood ratio

homo_sapiens GRCh38 VARIANT 0.0.1-a7b13bb
Inspect
/ asc
Public

ASC autism case/control exome results

homo_sapiens GRCh38 VARIANT 0.0.1-20210812
Inspect
/ qatar
Public

Qatari Genome allele frequencies

homo_sapiens GRCh38 VARIANT 0.0.1-20180529
Inspect
/ pangolin
Public

Pangolin masked splice gain/loss scores

homo_sapiens GRCh38 VARIANT 0.0.1-20250612
Inspect
/ wbbc
Public

Westlake BioBank for Chinese allele frequencies

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ turkish_variome
Public

Turkish Variome allele frequencies

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ tommo61kjpn
Public

ToMMo 61KJPN allele frequencies

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ popeve
Public

popEVE proteome-wide missense pathogenicity score

homo_sapiens GRCh38 VARIANT 0.0.1-20250715
Inspect
/ abraom
Public

ABraOM/SABE allele frequencies

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ func_vep
Public

FuncVEP-CTI missense variant effect score

homo_sapiens GRCh38 VARIANT 0.0.3-20260826
Inspect
/ dbsnp
Public

dbSNP

homo_sapiens GRCh38 VARIANT 0.0.1-157-202609
Inspect
/ alphagenome_avi
Public

AlphaGenome Atlas Variant Impact (AVI) PHRED score

homo_sapiens GRCh38 VARIANT 0.0.1-20260908
Inspect
/ alfa
Public

ALFA: Allele Frequency Aggregator

homo_sapiens GRCh38 VARIANT 0.0.3-20260205170148
Inspect
/ mitomap_polymorphisms
Public

Mitomap Polymorphisms

homo_sapiens GRCh38 VARIANT 0.0.3-20260802
Inspect
/ mitomap_disease
Public

Mitomap Disease

homo_sapiens GRCh38 VARIANT 0.0.3-20260802
Inspect
/ civic
Public

CivicDB

homo_sapiens GRCh38 VARIANT 0.0.2-20260423
Inspect
/ promoterai
Public

PromoterAI

homo_sapiens GRCh38 VARIANT 0.0.3
Inspect
/ gnomad_mnv_coding_hg38
Public

Genome Aggregation Database Exomes MNV Coding AF

homo_sapiens GRCh38 VARIANT 0.0.2-2.1.1
Inspect
/ gnomad_sv4
Public

Genome Aggregation Database Structural Variants 4.1.0, GRCh38,

homo_sapiens GRCh38 STRUCTURAL_VARIANT 0.0.3-4.1.0
Inspect
/ dvd_hg38
Public

Deafness Variation Database hg38

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ dbscsnv_hg38
Public

dbscSNV1.1 hg38

homo_sapiens GRCh38 VARIANT 0.0.2-1.1
Inspect
/ splicevardb_hg38
Public

SpliceVarDB HG38

homo_sapiens GRCh38 VARIANT 0.0.2
Inspect
/ gnomad_genomes4
Public

Genome Aggregation Database Genomes 4.1.0, GRCh38,

homo_sapiens GRCh38 VARIANT 0.0.4-4.1.0
Inspect
/ gnomad_exomes_depth
Public

Depth of the GnomAD Exomes

homo_sapiens GRCh38 POSITION 0.0.1-4.1.0
Inspect
/ gnomad_genomes3
Public

Genome Aggregation Database Genomes 3, GRCh38,

homo_sapies GRCh38 VARIANT 0.0.1-3.1.2
Inspect
/ gnomad_exomes4
Public

Genome Aggregation Database Exomes 4.1.0, GRCh38,

homo_sapiens GRCh38 VARIANT 0.0.4-4.1.0
Inspect
/ gnomad_total4
Public

Genome Aggregation Database Genomes and Exomes 4.1.0, GRCh38,

homo_sapiens GRCh38 VARIANT 0.0.4-4.1.0
Inspect
/ gpn_msa
Public

GPN-MSA - genomic pretrained network with multiple-sequence alignment

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ mutation_taster_hg38
Public

Precomputed MutationTaster 2021 Annotations for Genetic Variant Interpretation hg38

homo_sapiens GRCh38 VARIANT 0.0.2-20250217
Inspect
/ mutsplicedb_hg38
Public

MutSpliceDB HG38

homo_sapiens GRCh38 VARIANT 0.0.1-20250326
Inspect
/ cardioboost_cardiomyopathies_hg19
Public

CardioBoost Cardiomyopathies

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ cardioboost_arrhythmias_hg19
Public

CardioBoost Arrhythmias

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ cardioboost_cardiomyopathies_hg38
Public

CardioBoost Cardiomyopathies

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ cardioboost_arrhythmias_hg38
Public

CardioBoost Arrhythmias

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ gnomad3_mito
Public

GnomAD Mitochondrial data

homo_sapiens GRCh38 VARIANT 0.0.1-3.1.2
Inspect
/ mitomap-disease
Public

Mitomap Disease

homo_sapiens GRCh38 VARIANT 0.0.1-20251004
Inspect
/ alpha_missense
Public

Title of alpha_missense

homo_sapiens GRCh38 VARIANT 0.2.2
Inspect
/ mitomap-polymorphisms
Public

Mitomap Polymorphisms

homo_sapiens GRCh38 VARIANT 0.0.1-20250928
Inspect
/ alpha-missense
Public

Title of alpha-missense

homo_sapiens GRCh38 VARIANT 0.2.2
Inspect
/ moalmanac
Public

Molecular Oncology Almanac

homo_sapiens GRCh38 VARIANT 0.0.1-20250901
Inspect
/ primateai3d
Public

PrimateAI_3D

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ gnomad-total4
Public DELETED

Genome Aggregation Database Genomes and Exomes 4.1.0, GRCh38,

homo_sapiens GRCh38 VARIANT 0.0.4-4.1.0
Inspect
/ gnomad-genomes4
Public DURING_UPLOAD

Genome Aggregation Database Genomes 4.1.0, GRCh38,

homo_sapiens GRCh38 VARIANT 0.0.4-4.1.0
Inspect
/ mutpred_hg38
Public

MutPred, GRCh38

homo_sapiens GRCh38 VARIANT 0.0.1-2
Inspect
/ mpc_hg38
Public

MPC, GRCh38

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ gnomad_exomes2_hg38
Public

Genome Aggregation Database Exomes 2.1.1, GRCh38,

homo_sapiens GRCh38 VARIANT 0.0.4-2.1.1
Inspect
/ dbscsnv-hg38
Public

dbscSNV1.1 hg38

homo_sapiens GRCh38 VARIANT 0.0.2-1.1
Inspect
/ dbscsnv-hg19
Public

dbscSNV1.1 hg19

homo_sapiens GRCh37 VARIANT 0.0.2-1.1
Inspect
/ gnomad-exomes4
Public

Genome Aggregation Database Exomes 4.1.0, GRCh38,

homo_sapies GRCh38 VARIANT 0.0.3-4.1.0
Inspect
/ cosmic-genomescreensmutant-hg19
Public DELETED

COSMIC v102 GenomeScreensMutant GRCh37

tmptable homo_sapiens VARIANT 0.0.1-102
Inspect
/ cosmic-genomescreensmutant-hg38
Public DELETED

COSMIC v102 GenomeScreensMutant GRCh38

tmptable homo_sapiens VARIANT 0.0.1-102
Inspect
/ gnomad_genomes2_hg38
Public

Genome Aggregation Database Genomes 2.1.1, GRCh38,

homo_sapies GRCh38 VARIANT 0.0.3-2.1.1
Inspect
/ gnomad_exomes2_hg19
Public

Genome Aggregation Database Exomes 2.1.1, GRCh37,

homo_sapies GRCh37 VARIANT 0.0.3-2.1.1
Inspect
/ gnomad_genomes2_hg19
Public

Genome Aggregation Database Genomes 2.1.1, GRCh37,

homo_sapies GRCh37 VARIANT 0.0.3-2.1.1
Inspect
/ varity_hg38
Public

VARITY

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ gnomad-exomes2
Public

Title of gnomad-exomes2

homo_sapiens GRCh38 VARIANT 0.0.2-2.1.1
Inspect
/ gnomad-genomes2
Public DELETED

Genome Aggregation Database Genomes 2.1.1, GRCh38,

homo_sapies GRCh38 VARIANT 0.0.2-2.1.1
Inspect
/ clinpred_hg19
Public

ClinPred hg19

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ clinpred_hg38
Public

ClinPred hg38

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ mutation-taster_hg38
Public

Precomputed MutationTaster 2021 Annotations for Genetic Variant Interpretation hg38

homo_sapiens GRCh38 VARIANT 0.0.2-20250217
Inspect
/ mutation-taster_hg19
Public

Precomputed MutationTaster 2021 Annotations for Genetic Variant Interpretation hg19

homo_sapiens GRCh37 VARIANT 0.0.2-20250217
Inspect
/ splicevardb-hg38
Public

SpliceVarDB HG38

homo_sapiens GRCh38 VARIANT 0.0.2
Inspect
/ cbioportal_hg38
Public

cBioPortal hg38

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ uk10k_hg19
Public

UK10K hg19

tmptable homo_sapiens VARIANT 0.0.1
Inspect
/ uk10k_hg38
Public

UK10K hg38

tmptable homo_sapiens VARIANT 0.0.1
Inspect
/ genomeasia100k_hg19
Public

Genome Asia 100k hg19

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ genomeasia100k_hg38
Public

Genome Asia 100k hg38

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ gnomad-genomes3
Public DELETED

Genome Aggregation Database Genomes 3, GRCh38,

homo_sapies GRCh38 VARIANT 0.0.1-3.1.2
Inspect
/ dvd-hg38
Public DELETED

Deafness Variation Database hg38

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ dvd-hg19
Public

Deafness Variation Database hg19

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ cadd_hg38
Public

CADD is a tool for scoring the deleteriousness

homo_sapiens GRCh38 VARIANT 0.0.2-1.7.0
Inspect
/ gnomad3-mito
Public

GnomAD Mitochondrial data

homo_sapiens GRCh38 VARIANT 0.0.1-3.1.2
Inspect
/ mutsplicedb-hg38
Public

MutSpliceDB HG38

homo_sapiens GRCh38 VARIANT 0.0.1-20250326
Inspect
/ helixmtdb
Public

HelixMtDB

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ cardioboost-cardiomyopathies-hg38
Public

CardioBoost Cardiomyopathies

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ cardioboost-cardiomyopathies-hg19
Public

CardioBoost Cardiomyopathies

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ cardioboost-arrhythmias-hg38
Public

CardioBoost Arrhythmias

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ cardioboost-arrhythmias-hg19
Public

CardioBoost Arrhythmias

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ gpn-msa
Public

GPN-MSA - genomic pretrained network with multiple-sequence alignment

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ mutation-taster
Public

Precomputed MutationTaster 2021 Annotations for Genetic Variant Interpretation

homo_sapiens GRCh37 VARIANT 0.0.1-20250217
Inspect
/ phastcons100_hg19
Public

phastCons100

homo_sapies GRCh37 POSITION 0.0.1
Inspect
/ phastcons100_hg38
Public

phastCons100

homo_sapies GRCh38 POSITION 0.0.1
Inspect
/ phylop100_hg38
Public

phylop100

homo_sapies GRCh38 POSITION 0.0.1
Inspect
/ phylop100_hg19
Public

phylop100

homo_sapies GRCh37 POSITION 0.0.1
Inspect
/ cadd_hg19
Public

CADD is a tool for scoring the deleteriousness

homo_sapiens GRCh37 VARIANT 0.0.2-1.7.0
Inspect
/ varity
Public

Improved pathogenicity prediction for rare human missense variants

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ ccrs_hg19
Public

Title of ccrs_hg19

homo_sapiens GRCh37 REGION 0.0.1
Inspect
/ ccrs_hg38
Public

Title of ccrs_hg38

homo_sapiens GRCh38 REGION 0.0.1
Inspect
/ gnomad3-genomes-depth
Public

Depth of the GnomAD3 Genomes

homo_sapiens GRCh38 POSITION 0.0.1-3.0.1
Inspect
/ phylop100way_hg19
Public DELETED

Conservation scores by phyloP, hg19

homo_sapiens GRCh37 POSITION 0.0.1
Inspect
/ phylop100way
Public DELETED

Conservation scoring by phyloP

homo_sapiens GRCh38 POSITION 0.0.1
Inspect
/ phylop100
Public DELETED

PhyloP scores conservation from 99 vertebrate alignments to human

homo_sapiens GRCh38 POSITION 0.0.1
Inspect
/ gnomad2-exomes-hg19
Public

GnomAD Exomes hg19, v. 2.1.1 - Genome Aggregation Database

homo_sapiens GRCh37 VARIANT 0.0.1-2.1.1
Inspect
/ gnomad2-genomes-hg19
Public

GnomAD Genomes hg19, v. 2 - Genome Aggregation Database

homo_sapiens GRCh37 VARIANT 0.0.1-2.0.0
Inspect
/ gnomad-exomes-depth
Public

Depth of the GnomAD Exomes

homo_sapiens GRCh38 POSITION 0.0.1-4.1.0
Inspect
/ revel_hg19
Public

REVEL hg19

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ revel
Public

REVEL - Rare Exome Variant Ensemble Learner

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ bayesdel_noaf
Public

BayesDel noAF

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ topmed
Public

Topmed

homo_sapiens GRCh38 VARIANT 0.0.1-freeze.8
Inspect
/ spliceai
Public

SOTA Splicing Variants impact predictions

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
/ dbsnp_hg19
Public

The Single Nucleotide Polymorphism Database, hg19

homo_sapiens GRCh37 VARIANT 0.0.1-156
Inspect
/ dann_hg19
Public

DANN: Deep Learning-Based Variant Annotation Database

homo_sapiens GRCh37 VARIANT 0.0.1
Inspect
/ gnomad-exomes
Public DELETED

GnomAD Exomes - Genome Aggregation Database

homo_sapiens GRCh38 VARIANT 0.0.1-4.1.0
Inspect
/ gnomad-genomes
Public DELETED

GnomAD Genomes - Genome Aggregation Database

homo_sapiens GRCh38 VARIANT 0.0.1-4.1.0
Inspect
/ dann_hg38
Public

DANN: Deep Learning-Based Variant Annotation Database, GRCh38 version

homo_sapiens GRCh38 VARIANT 0.0.1
Inspect
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