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Items: 1 to 20 of 200

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056628inversion1nstd229human GRCh38 chr7: 95,496,336-95,496,378 , GRCh37.p13 chr7: 95,125,648-95,125,690 ASB4
    nsv7056243inversion1nstd229human GRCh38 chr7: 95,228,264-96,257,993 , GRCh37.p13 chr7: 94,857,576-95,887,305 PON2, LOC107986823, 14 more genes
    nsv7050278inversion1nstd229human GRCh38 chr7: 92,907,694-98,049,952 , GRCh37.p13 chr7: 92,537,008-97,679,264 LOC105375416, RNU6-364P, 88 more genes
    nsv7044141inversion1nstd229human GRCh38 chr7: 89,303,967-95,903,508 , GRCh37.p13 chr7: 88,933,281-95,532,820 MIR4652, PPP1R9A-AS1, 94 more genes
    nsv7039444inversion1nstd229human GRCh38 chr7: 95,498,510-95,511,036 , GRCh37.p13 chr7: 95,127,822-95,140,348 ASB4
    nsv6827917copy number variation1nstd229human GRCh38 chr7: 95,521,691-95,673,473 , GRCh37.p13 chr7: 95,151,003-95,302,785 LOC107986746, PDK4-AS1, 3 more genes
    nsv6827171copy number variation1nstd229human GRCh38 chr7: 95,449,121-95,483,529 , GRCh37.p13 chr7: 95,078,433-95,112,841 LOC107986823, ASB4
    nsv6825854copy number variation1nstd229human GRCh38 chr7: 95,501,001-95,511,100 , GRCh37.p13 chr7: 95,130,313-95,140,412 ASB4
    nsv6823383copy number variation1nstd229human GRCh38 chr7: 95,487,956-95,619,979 , GRCh37.p13 chr7: 95,117,268-95,249,291 PDK4-AS1, PDK4, 1 more genes
    nsv6819645copy number variation1nstd229human GRCh38 chr7: 95,493,301-95,559,800 , GRCh37.p13 chr7: 95,122,613-95,189,112 ASB4
    nsv6636271copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225 MARK2P10, PON2, 97 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
    nsv6632409copy number variation1nstd224human GRCh37 chr7: 95,119,261-95,249,224 , GRCh38.p12 chr7: 95,489,949-95,619,912 PDK4-AS1, PDK4, 1 more genes
    nsv6612325copy number variation1nstd223human GRCh38 chr7: 95,537,601-95,541,800 , GRCh37.p13 chr7: 95,166,913-95,171,112 ASB4
    nsv6563930inversion1nstd223human GRCh38 chr7: 95,499,651-95,500,479 , GRCh37.p13 chr7: 95,128,963-95,129,791 ASB4
    nsv6559056inversion1nstd223human GRCh38 chr7: 95,499,721-95,500,706 , GRCh37.p13 chr7: 95,129,033-95,130,018 ASB4
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6239477mobile element insertion1nstd215human GRCh38 chr7: 95,513,333-95,513,333 , GRCh37.p13 chr7: 95,142,645-95,142,645 ASB4
    nsv6137024copy number variation1nstd213human GRCh37 chr7: 93,400,000-97,690,001 , GRCh38.p12 chr7: 93,770,688-98,060,689 , SEM1, 77 more genes
    nsv6136216copy number variation1nstd213human GRCh37 chr7: 95,100,000-95,260,001 , GRCh38.p12 chr7: 95,470,688-95,630,689 PDK4, ASB4, 2 more genes
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