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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7057176inversion1nstd229human GRCh38 chr7: 142,200,564-149,795,026 , GRCh37.p13 chr7: 141,988,816-149,492,114 RN7SL72P, RPL32P17, 258 more genes
    nsv7046837inversion1nstd229human GRCh38 chr7: 146,996,779-152,901,438 , GRCh37.p13 chr7: 146,693,871-152,598,523 RARRES2, RN7SL76P, 153 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6570634inversion1nstd223human GRCh38 chr7: 149,482,706-149,483,488 , GRCh37.p13 chr7: 149,179,797-149,180,579 ZNF746
    nsv6568527inversion1nstd223human GRCh38 chr7: 149,482,584-149,483,520 , GRCh37.p13 chr7: 149,179,675-149,180,611 ZNF746
    nsv6558115inversion1nstd223human GRCh38 chr7: 146,996,771-152,901,398 , GRCh37.p13 chr7: 146,693,863-152,598,483 ZNF398, PRKAG2-AS1, 153 more genes
    nsv6424243copy number variation1nstd223human GRCh38 chr7: 149,485,851-149,489,497 , GRCh37.p13 chr7: 149,182,942-149,186,588 ZNF746
    nsv6422436copy number variation1nstd223human GRCh38 chr7: 149,474,301-149,476,400 , GRCh37.p13 chr7: 149,171,392-149,173,491 ZNF746
    nsv6420257copy number variation1nstd223human GRCh38 chr7: 149,408,401-149,486,200 , GRCh37.p13 chr7: 149,105,492-149,183,291 TRC-GCA11-1, ZNF777, 1 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6315172copy number variation1nstd102humanPathogenic GRCh37 chr7: 149,062,717-159,124,131 , GRCh38.p12 chr7: 149,365,626-159,331,441 KCNH2, SLC4A2, 191 more genes
    nsv6315169copy number variation1nstd102humanPathogenic GRCh37 chr7: 146,927,174-159,128,556 , GRCh38.p12 chr7: 147,230,082-159,335,866 LOC105375554, ATP5PBP3, 233 more genes
    nsv6291241copy number variation1nstd102humanPathogenic GRCh37 chr7: 148,153,261-157,543,640 , GRCh38.p12 chr7: 148,456,169-157,750,948 TRC-GCA23-1, HTR5A-AS1, 210 more genes
    nsv6291163copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,851,002-159,119,707 , GRCh38.p12 chr7: 134,166,250-159,327,017 TRB, ZC3HAV1L, 579 more genes
    nsv6290897copy number variation1nstd102humanPathogenic GRCh37 chr7: 148,695,373-159,119,707 , GRCh38.p12 chr7: 148,998,281-159,327,017 TRC-GCA21-1, LINC00996, 209 more genes
    nsv6136973copy number variation1nstd213human GRCh37 chr7: 149,040,000-149,330,001 , GRCh38.p12 chr7: 149,342,909-149,632,910 ZNF767P, TRC-GCA11-1, 16 more genes
    nsv6136972copy number variation1nstd213human GRCh37 chr7: 146,490,000-151,820,001 , GRCh38.p12 chr7: 146,792,908-152,122,916 AOC1, KCNH2, 140 more genes
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