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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7055390inversion1nstd229human GRCh38 chr7: 100,184,977-102,400,588 , GRCh37.p13 chr7: 99,782,600-101,718,950 SLC12A9-AS1, STAG3, 84 more genes
    nsv7051497inversion1nstd229human GRCh38 chr7: 100,869,983-101,245,444 , GRCh37.p13 chr7: 100,467,605-100,888,725 MUC12, FIS1, 23 more genes
    nsv7041641inversion1nstd229human GRCh38 chr7: 101,083,186-101,090,273 , GRCh37.p13 chr7: 100,726,467-100,733,554 TRIM56
    nsv6826957copy number variation1nstd229human GRCh38 chr7: 100,918,010-102,186,129 , GRCh37.p13 chr7: 100,515,630-101,718,950 COL26A1, AP1S1, 28 more genes
    nsv6820511copy number variation1nstd229human GRCh38 chr7: 100,411,473-102,072,572 , GRCh37.p13 chr7: 100,009,096-101,715,852 MIR4653, UFSP1, 63 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
    nsv6631717copy number variation1nstd224human GRCh37 chr7: 100,647,920-100,731,027 , GRCh38.p12 chr7: 101,004,639-101,087,746 MUC17, TRIM56, 3 more genes
    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
    nsv6612277copy number variation1nstd223human GRCh38 chr7: 101,084,117-101,093,175 , GRCh37.p13 chr7: 100,727,398-100,736,456 TRIM56
    nsv6604708copy number variation1nstd223human GRCh38 chr7: 100,460,230-101,238,868 , GRCh37.p13 chr7: 100,057,853-100,882,149 RN7SKP54, ZNHIT1, 49 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 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
    nsv6177433copy number variation1nstd214human GRCh38 chr7: 101,097,896-101,097,962 , GRCh37.p13 chr7: 100,741,177-100,741,243 TRIM56
    nsv6136529copy number variation1nstd213human GRCh37 chr7: 100,110,000-100,860,001 , GRCh38.p12 chr7: 100,512,377-101,216,720 ACHE, AP1S1, 44 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
    nsv6107847inversion1nstd212human GRCh38 chr7: 100,184,978-102,378,892 , GRCh37.p13 chr7: 99,782,601-101,718,950 , ACHE, 87 more genes
    nsv6101547inversion1nstd212human GRCh38 chr7: 98,453,223-101,264,028 , GRCh37.p13 chr7: 98,082,535-100,907,309 , ACHE, 141 more genes
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