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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148151copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,486,532-37,745,203 , GRCh37.p13 chr17: 34,900,240-35,888,667 PIGW, LOC105371751, 32 more genes
    nsv7148119copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,752,221-36,105,007 , GRCh38.p12 chr17|NT_187614.1: 694,163-1,984,072 , GRCh38.p12 chr17: 36,446,545-37,745,016 LOC105371756, SYNRG, 35 more genes
    nsv7137104copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,842,545-36,293,050 , GRCh38.p12 chr17: 36,486,701-37,933,506 , GRCh38.p12 chr17|NT_187614.1: 721,605-2,172,115 LHX1-DT, LOC105371749, 40 more genes
    nsv7098907copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,138,501-37,924,067 , GRCh37.p13 chr17: 34,900,240-35,888,667 LOC102723414, SYNRG, 51 more genes
    nsv7098735copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 34,842,542-36,104,877 , GRCh38.p12 chr17: 36,486,698-37,744,886 , GRCh38.p12 chr17|NT_187614.1: 721,602-1,983,942 ACACA, LHX1, 34 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv7070483inversion1nstd229human GRCh38 chr17: 36,507,875-36,562,214 , GRCh37.p13 chr17|NW_003315949.1: 392,625-429,138 GGNBP2, MYO19, 1 more genes
    nsv7069606inversion1nstd229human GRCh38 chr17: 36,513,194-36,513,226 , GRCh37.p13 chr17|NW_003315949.1: 397,944-397,976 MYO19
    nsv7064857inversion1nstd229human GRCh38 chr17: 36,496,730-36,501,385 , GRCh37.p13 chr17|NW_003315949.1: 381,480-386,135 ZNHIT3, MYO19
    nsv7063878inversion1nstd229human GRCh38 chr17: 36,492,269-36,496,831 , GRCh37.p13 chr17|NW_003315949.1: 377,019-381,581 ZNHIT3, MYO19
    nsv6991238copy number variation1nstd229human GRCh38 chr17: 36,512,042-36,520,053 , GRCh37.p13 chr17|NW_003315949.1: 396,792-404,801 MYO19
    nsv6982458copy number variation1nstd229human GRCh38 chr17: 36,527,459-36,530,174 , GRCh37.p13 chr17|NW_003315949.1: 412,207-414,922 MYO19
    nsv6979790copy number variation1nstd229human GRCh38 chr17: 36,523,645-36,523,715 , GRCh37.p13 chr17|NW_003315949.1: 408,393-408,463 MYO19
    nsv6637369copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,425,363-36,404,555 , GRCh38.p12 chr17|NT_187614.1: 332,891-2,283,620 CCL3L3, MRM1, 63 more genes
    nsv6634438copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,842,544-36,104,875 , GRCh38.p12 chr17: 36,486,700-37,744,884 , GRCh38.p12 chr17|NT_187614.1: 721,604-1,983,940 HNF1B, LOC100419621, 34 more genes
    nsv6634420copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,822,465-36,243,781 , GRCh38.p12 chr17|NT_187614.1: 701,523-2,122,846 , GRCh38.p12 chr17: 36,466,619-37,884,161 GGNBP2, AATF, 36 more genes
    nsv6624272copy number variation1nstd224human GRCh37 chr17: 34,815,551-36,249,430 , GRCh38.p12 chr17: 36,459,737-37,889,808 , GRCh38.p12 chr17|NT_187614.1: 694,641-2,128,495 DDX52, DUSP14, 36 more genes
    nsv6624076copy number variation1nstd224human GRCh37 chr17: 34,815,551-34,854,280 , GRCh38.p12 chr17: 36,459,737-36,498,436 , GRCh38.p12 chr17|NT_187614.1: 694,641-733,340 LOC105371749, MYO19, 2 more genes
    nsv6623850copy number variation1nstd224human GRCh37 chr17: 34,815,551-36,411,684 , GRCh38.p12 chr17|NT_187614.1: 694,641-2,290,749 LHX1, HNF1B, 44 more genes
    nsv6589348inversion1nstd223human GRCh38 chr17: 36,518,793-36,519,600 , GRCh37.p13 chr17|NW_003315949.1: 403,541-404,348 MYO19
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