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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070638inversion1nstd229human GRCh38 chr17: 20,843,363-22,437,673 , GRCh37.p13 chr17: 20,746,676-21,937,002 LOC107987246, PDLIM1P2, 33 more genes
    nsv7066202inversion1nstd229human GRCh38 chr17: 21,136,031-21,139,457 , GRCh37.p13 chr17: 21,039,344-21,042,770 DHRS7B
    nsv6994560copy number variation1nstd229human GRCh38 chr17: 21,179,785-21,180,073 , GRCh37.p13 chr17: 21,083,098-21,083,386 DHRS7B
    nsv6993786copy number variation1nstd229human GRCh38 chr17: 21,153,560-21,166,559 , GRCh37.p13 chr17: 21,056,873-21,069,872 DHRS7B
    nsv6992852copy number variation1nstd229human GRCh38 chr17: 21,148,417-21,152,173 , GRCh37.p13 chr17: 21,051,730-21,055,486 DHRS7B
    nsv6989111copy number variation1nstd229human GRCh38 chr17: 21,170,528-21,171,669 , GRCh37.p13 chr17: 21,073,841-21,074,982 DHRS7B
    nsv6979075copy number variation1nstd229human GRCh38 chr17: 21,146,152-21,154,078 , GRCh37.p13 chr17: 21,049,465-21,057,391 DHRS7B
    nsv6595125inversion1nstd223human GRCh38 chr17: 21,187,609-21,187,767 , GRCh37.p13 chr17: 21,090,922-21,091,080 DHRS7B
    nsv6588161inversion1nstd223human GRCh38 chr17: 21,139,648-21,140,031 , GRCh37.p13 chr17: 21,042,961-21,043,344 DHRS7B
    nsv6586706inversion1nstd223human GRCh38 chr17: 21,122,583-21,123,962 , GRCh37.p13 chr17: 21,025,896-21,027,275 DHRS7B
    nsv6581021inversion1nstd223human GRCh38 chr17: 21,151,225-21,152,424 , GRCh37.p13 chr17: 21,054,538-21,055,737 DHRS7B
    nsv6578618inversion1nstd223human GRCh38 chr17: 21,187,643-21,188,135 , GRCh37.p13 chr17: 21,090,956-21,091,448 DHRS7B
    nsv6510629copy number variation1nstd223human GRCh38 chr17: 21,128,217-21,128,636 , GRCh37.p13 chr17: 21,031,530-21,031,949 DHRS7B
    nsv6510484copy number variation1nstd223human GRCh38 chr17: 21,153,560-21,166,554 , GRCh37.p13 chr17: 21,056,873-21,069,867 DHRS7B
    nsv6507665copy number variation1nstd223human GRCh38 chr17: 21,134,077-21,134,510 , GRCh37.p13 chr17: 21,037,390-21,037,823 DHRS7B
    nsv6502353copy number variation1nstd223human GRCh38 chr17: 21,111,202-21,303,044 , GRCh37.p13 chr17: 21,014,515-21,206,356 EIF1P5, MAP2K3, 5 more genes
    nsv6496025copy number variation1nstd223human GRCh38 chr17: 21,179,793-21,180,073 , GRCh37.p13 chr17: 21,083,106-21,083,386 DHRS7B
    nsv6315238complex substitution1nstd102humanPathogenic GRCh37 chr17: 14,876,984-22,124,952 , GRCh38.p12 chr17: 14,973,667-22,625,625 ADORA2B, ALDH3A1, 281 more genes
    nsv6250694mobile element insertion1nstd215human GRCh38 chr17: 21,152,972-21,152,972 , GRCh37.p13 chr17: 21,056,285-21,056,285 DHRS7B
    nsv6133347copy number variation1nstd213human GRCh37 chr17: 20,600,000-21,090,001 , GRCh38.p12 chr17: 20,696,687-21,186,688 USP22, DHRS7B, 12 more genes
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