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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099198copy number variation1nstd231human GRCh38.p12 chr1: 44,129,375-46,768,878 , GRCh37 chr1: 44,595,047-47,234,550 PLK3, FAAH, 93 more genes
    nsv7095531copy number variation1nstd102humanUncertain significance GRCh37 chr1: 44,257,753-46,663,493 , GRCh38.p12 chr1: 43,792,082-46,197,821 AKR1A1, OSTCP5, 87 more genes
    nsv7055071inversion1nstd229human GRCh38 chr1: 43,970,005-47,371,780 , GRCh37.p13 chr1: 44,435,677-47,837,452 SNORD38A, PPIAP36, 121 more genes
    nsv7046201inversion1nstd229human GRCh38 chr1: 45,964,231-47,257,863 , GRCh37.p13 chr1: 46,429,903-47,723,535 TUBAP9, MKNK1-AS1, 45 more genes
    nsv6650756copy number variation1nstd229human GRCh38 chr1: 46,175,972-46,196,094 , GRCh37.p13 chr1: 46,641,644-46,661,766 POMGNT1, P3R3URF, 2 more genes
    nsv6650755copy number variation1nstd229human GRCh38 chr1: 46,175,085-46,179,132 , GRCh37.p13 chr1: 46,640,757-46,644,804 P3R3URF, P3R3URF-PIK3R3, 2 more genes
    nsv6650678copy number variation1nstd229human GRCh38 chr1: 46,144,772-46,208,450 , GRCh37.p13 chr1: 46,610,444-46,674,122 LURAP1, P3R3URF, 4 more genes
    nsv6650650copy number variation1nstd229human GRCh38 chr1: 45,756,413-46,218,248 , GRCh37.p13 chr1: 46,222,085-46,683,920 P3R3URF-PIK3R3, MAST2, 10 more genes
    nsv6650649copy number variation1nstd229human GRCh38 chr1: 45,728,361-46,294,276 , GRCh37.p13 chr1: 46,194,033-46,759,948 POMGNT1, LOC105378694, 13 more genes
    nsv6650541copy number variation1nstd229human GRCh38 chr1: 45,962,193-46,235,324 , GRCh37.p13 chr1: 46,427,865-46,700,996 LOC101929626, MAST2, 6 more genes
    nsv6650019copy number variation1nstd229human GRCh38 chr1: 46,155,838-46,286,125 , GRCh37.p13 chr1: 46,621,510-46,751,797 RAD54L, LRRC41, 6 more genes
    nsv6650013copy number variation1nstd229human GRCh38 chr1: 45,981,011-46,246,158 , GRCh37.p13 chr1: 46,446,683-46,711,830 P3R3URF, LURAP1, 7 more genes
    nsv6636290copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,233,623-46,668,497 , GRCh38.p12 chr1: 45,767,951-46,202,825 TMA16P2, P3R3URF, 9 more genes
    nsv6323355copy number variation1nstd223human GRCh38 chr1: 46,159,381-46,205,659 , GRCh37.p13 chr1: 46,625,053-46,671,331 TSPAN1, P3R3URF, 4 more genes
    nsv6313850copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,083,531-46,738,006 , GRCh38.p12 chr1: 45,617,859-46,272,334 LOC105378694, POMGNT1, 18 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6290563copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,098,762-46,668,497 , GRCh38.p12 chr1: 45,633,090-46,202,825 LURAP1, POMGNT1, 15 more genes
    nsv5563104sequence alteration1nstd206human GRCh38 chr1: 45,733,110-46,239,402 , GRCh37.p13 chr1: 46,198,782-46,705,074 IPP, LOC101929626, 11 more genes
    nsv4906329copy number variation1nstd200human GRCh38 chr1: 46,175,085-46,179,127 , GRCh37.p13 chr1: 46,640,757-46,644,799 TSPAN1, PIK3R3, 2 more genes
    nsv4903449copy number variation1nstd200human GRCh38 chr1: 46,152,857-46,274,186 , GRCh37.p13 chr1: 46,618,529-46,739,858 POMGNT1, LURAP1, 5 more genes
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