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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 LAMTOR4, PTCD1, 107 more genes
    nsv7098147copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,507,659-100,860,555 , GRCh38.p12 chr7: 98,910,036-101,217,274 SLC12A9, LOC105375423, 127 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv6833074copy number variation1nstd229human GRCh38 chr7: 100,051,530-100,054,490 , GRCh37.p13 chr7: 99,649,153-99,652,113 ZSCAN21
    nsv6832061copy number variation1nstd229human GRCh38 chr7: 100,048,149-100,056,487 , GRCh37.p13 chr7: 99,645,772-99,654,110 ZSCAN21
    nsv6826407copy number variation1nstd229human GRCh38 chr7: 100,050,901-100,054,500 , GRCh37.p13 chr7: 99,648,524-99,652,123 ZSCAN21
    nsv6820388copy number variation1nstd229human GRCh38 chr7: 100,051,526-100,054,468 , GRCh37.p13 chr7: 99,649,149-99,652,091 ZSCAN21
    nsv6818377copy number variation1nstd229human GRCh38 chr7: 100,055,422-100,059,999 , GRCh37.p13 chr7: 99,653,045-99,657,622 ZSCAN21
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6618066copy number variation1nstd223human GRCh38 chr7: 100,051,301-100,054,500 , GRCh37.p13 chr7: 99,648,924-99,652,123 ZSCAN21
    nsv6614776copy number variation1nstd223human GRCh38 chr7: 99,943,801-101,566,300 , GRCh37.p13 chr7: 99,541,424-101,209,580 MUC12, FBXO24, 95 more genes
    nsv6607029copy number variation1nstd223human GRCh38 chr7: 100,055,430-100,059,992 , GRCh37.p13 chr7: 99,653,053-99,657,615 ZSCAN21
    nsv6568514inversion1nstd223human GRCh38 chr7: 100,059,566-100,060,480 , GRCh37.p13 chr7: 99,657,189-99,658,103 ZSCAN21
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
    nsv6312372copy number variation1nstd102humanPathogenic GRCh37 chr7: 98,983,338-100,860,555 , GRCh38.p12 chr7: 99,385,715-101,217,274 AZGP1P1, MOGAT3, 119 more genes
    nsv6290864copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,755,291-99,886,571 , GRCh38.p12 chr7: 99,157,668-100,288,948 LAMTOR4, OR2AE1, 62 more genes
    nsv6136217copy number variation1nstd213human GRCh37 chr7: 99,390,000-104,070,001 , GRCh38.p12 chr7: 99,792,377-104,429,553 AZGP1, CRYZP1, 157 more genes
    nsv6101547inversion1nstd212human GRCh38 chr7: 98,453,223-101,264,028 , GRCh37.p13 chr7: 98,082,535-100,907,309 , ACHE, 141 more genes
    nsv5979182inversion1nstd209human GRCh38 chr7: 99,981,419-101,289,122 , GRCh37.p13 chr7: 99,579,042-100,932,403 , ACHE, 92 more genes
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