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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141018copy number variation1nstd232human GRCh37.p13 chr7: 100,486,000-100,486,089 , GRCh38.p12 chr7: 100,888,379-100,888,468 ACHE, SRRT, 1 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
    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
    nsv6833153copy number variation1nstd229human GRCh38 chr7: 100,893,135-100,894,048 , GRCh37.p13 chr7: 100,490,756-100,491,669 ACHE
    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
    nsv6818312copy number variation1nstd229human GRCh38 chr7: 100,547,001-100,919,000 , GRCh37.p13 chr7: 100,144,624-100,516,620 TRIP6, MIR6875, 24 more genes
    nsv6635751copy number variation1nstd227human GRCh37 chr7: 100,492,127-100,492,896 , GRCh38.p12 chr7: 100,894,506-100,895,275 ACHE
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631716copy number variation1nstd224human GRCh37 chr7: 100,279,988-100,548,261 , GRCh38.p12 chr7: 100,682,365-100,950,627 ZAN, UFSP1, 15 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
    nsv6610199copy number variation1nstd223human GRCh38 chr7: 100,694,401-100,976,100 , GRCh37.p13 chr7: 100,292,024-100,619,381 MUC3A, ZAN, 16 more genes
    nsv6607668copy number variation1nstd223human GRCh38 chr7: 100,428,001-100,907,900 , GRCh37.p13 chr7: 100,025,624-100,505,520 LOC107986829, FBXO24, 33 more genes
    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
    nsv6601439copy number variation1nstd223human GRCh38 chr7: 100,412,401-100,918,900 , GRCh37.p13 chr7: 100,010,024-100,516,520 TSC22D4, NYAP1, 33 more genes
    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
    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
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