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Items: 1 to 20 of 208

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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
    nsv7148154copy number variation1nstd102humanPathogenic GRCh38 chr7: 154,446,117-159,206,757 , GRCh37.p13 chr7: 154,143,202-158,999,446 LOC105375602, LOC105375599, 70 more genes
    nsv7137106copy number variation1nstd102humanUncertain significance GRCh37 chr7: 154,633,174-155,446,847 , GRCh38.p12 chr7: 154,841,464-155,654,153 RBM33, RBM33-DT, 21 more genes
    nsv7097356copy number variation2nstd102humanPathogenic GRCh37 chr7: 152,617,597-158,500,659 , GRCh38.p12 chr7: 152,920,512-158,707,968 LOC107986722, LOC105375593, 76 more genes
    nsv6834999copy number variation1nstd229human GRCh38 chr7: 155,304,194-155,304,620 , GRCh37.p13 chr7: 155,095,904-155,096,330 INSIG1
    nsv6834022copy number variation1nstd229human GRCh38 chr7: 154,808,210-155,712,129 , GRCh37.p13 chr7: 154,599,920-155,504,823 RBM33, LOC105375594, 21 more genes
    nsv6824525copy number variation1nstd229human GRCh38 chr7: 152,687,878-156,500,924 , GRCh37.p13 chr7: 152,384,963-156,293,618 RN7SKP280, LINC03010, 44 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
    nsv6315413copy number variation1nstd102humanPathogenic GRCh37 chr7: 154,831,466-156,356,088 , GRCh38.p12 chr7: 155,039,756-156,563,394 SHH, INSIG1, 27 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
    nsv6135981copy number variation1nstd213human GRCh37 chr7: 154,760,000-155,230,001 , GRCh38.p12 chr7: 154,968,290-155,437,306 HTR5A, BLACE, 14 more genes
    nsv6135980copy number variation1nstd213human GRCh37 chr7: 154,380,000-159,138,663 , GRCh38.p12 chr7: 154,588,290-159,335,973 DPP6, INSIG1, 71 more genes
    nsv6135908copy number variation1nstd213human GRCh37 chr7: 154,510,000-159,138,663 , GRCh38.p12 chr7: 154,718,290-159,335,973 EN2, VIPR2, 70 more genes
    nsv6135747copy number variation1nstd213human GRCh37 chr7: 154,910,000-155,210,001 , GRCh38.p12 chr7: 155,118,290-155,417,306 INSIG1, LOC105375589, 10 more genes
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