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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914114copy number variation1nstd209human GRCh38 chr8: 143,808,341-143,808,422 , GRCh37.p13 chr8|NW_003315923.1: 146,986-147,067 , GRCh37.p13 chr8: 144,890,511-144,890,592 SCRIB
    nsv5641723insertion1nstd207human GRCh38 chr8: 143,808,288-143,808,288 , GRCh37.p13 chr8: 144,890,458-144,890,458 , GRCh37.p13 chr8|NW_003315923.1: 146,933-146,933 SCRIB
    nsv5631136insertion1nstd207human GRCh38 chr8: 143,808,399-143,808,399 , GRCh37.p13 chr8: 144,890,569-144,890,569 , GRCh37.p13 chr8|NW_003315923.1: 147,044-147,044 SCRIB
    nsv5301183copy number variation1nstd204human GRCh38.p13 chr8: 143,160,494-143,803,360 , GRCh37.p13 chr8: 144,241,911-144,743,529 TIGD5, MAPK15, 36 more genes
    nsv5254948copy number variation1nstd204human GRCh38.p13 chr8: 143,167,001-143,860,200 , GRCh37.p13 chr8: 144,248,418-144,743,525 LOC105375798, LINC02990, 41 more genes
    nsv5247240copy number variation1nstd204human GRCh38.p13 chr8: 143,641,501-143,860,200 , GRCh37.p13 chr8|NW_003315923.1: 1-198,845 , GRCh37.p13 chr8: 144,744,709-144,940,217 LOC105375799, FAM83H, 16 more genes
    nsv5241991copy number variation1nstd204human GRCh37.p13 chr8|NW_003315923.1: 89,346-217,145 , GRCh37.p13 chr8: 144,832,871-144,952,668 , GRCh38.p13 chr8: 143,750,701-143,878,500 PUF60, SCRIB, 7 more genes
    nsv4962661copy number variation1nstd200human GRCh38 chr8: 143,811,704-143,814,421 , GRCh37.p13 chr8|NW_003315923.1: 150,349-153,066 SCRIB, PUF60, 1 more genes
    nsv4962660copy number variation1nstd200human GRCh38 chr8: 143,801,864-143,803,185 , GRCh37.p13 chr8: 144,884,034-144,885,355 , GRCh37.p13 chr8|NW_003315923.1: 140,509-141,830 SCRIB
    nsv4962659copy number variation1nstd200human GRCh38 chr8: 143,796,624-143,797,687 , GRCh37.p13 chr8: 144,878,794-144,879,857 , GRCh37.p13 chr8|NW_003315923.1: 135,269-136,332 SCRIB
    nsv4813899copy number variation1nstd200human GRCh37 chr8: 144,893,874-144,896,591 , GRCh38.p12 chr8|NT_187571.1: 288,751-291,468 , GRCh38.p12 chr8: 143,811,704-143,814,421 SCRIB, MIR937, 1 more genes
    nsv4813898copy number variation1nstd200human GRCh37 chr8: 144,878,794-144,879,857 , GRCh38.p12 chr8|NT_187571.1: 273,671-274,734 , GRCh38.p12 chr8: 143,796,624-143,797,687 SCRIB
    nsv4761052insertion1nstd199human GRCh37 chr8: 144,890,510-144,890,510 , GRCh38.p12 chr8: 143,808,340-143,808,340 , GRCh38.p12 chr8|NT_187571.1: 285,387-285,387 SCRIB
    nsv4729603copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385 CYC1, EEF1D, 112 more genes
    nsv4676049copy number variation1nstd102humanPathogenic GRCh37 chr8: 143,616,831-144,930,611 , GRCh38.p12 chr8: 142,535,470-143,848,439 PYCR3, MROH4P, 69 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4675029copy number variation1nstd102humanPathogenic GRCh37 chr8: 142,132,678-145,569,441 , GRCh38.p12 chr8: 141,122,579-144,345,779 RHPN1-AS1, MIR6847, 117 more genes
    nsv4600370copy number variation1nstd183human GRCh37 chr8: 144,886,972-144,887,134 , GRCh38.p12 chr8: 143,804,802-143,804,964 , GRCh38.p12 chr8|NT_187571.1: 281,849-282,011 SCRIB
    nsv4485565mobile element insertion1nstd166human GRCh37.p13 chr8: 144,878,247-144,878,247 , GRCh38.p12 chr8: 143,796,077-143,796,077 , GRCh38.p12 chr8|NT_187571.1: 273,124-273,124 SCRIB
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