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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2667872copy number variation147estd199human GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952 DNAH14
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2676981copy number variation78estd199human GRCh37 chr19: 41,345,203-41,375,827 , GRCh38.p12 chr19: 40,839,298-40,869,922 CYP2A6
    esv2663673copy number variation27estd199human GRCh37 chr13: 57,865,913-57,892,004 , GRCh38.p12 chr13: 57,291,779-57,317,870 SLC25A5P4
    esv2661915copy number variation81estd199human GRCh37 chr6: 77,437,226-77,458,987 , GRCh38.p12 chr6: 76,727,509-76,749,270 LOC105377861
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2658667copy number variation23estd199human GRCh37 chr10: 122,769,645-122,788,992 , GRCh38.p12 chr10: 121,010,132-121,029,479 LOC105378521
    esv2662007copy number variation32estd199human GRCh37 chr10: 122,769,701-122,787,511 , GRCh38.p12 chr10: 121,010,188-121,027,998 LOC105378521
    esv2671077copy number variation44estd199human GRCh37 chr2: 180,065,450-180,081,661 , GRCh38.p12 chr2: 179,200,723-179,216,934 SESTD1
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2670787copy number variation158estd199human GRCh37 chr7: 151,134-160,557 , GRCh38.p12 chr7: 151,134-160,557 , GRCh38.p12 chr7|NT_187558.1: 106,939-119,904 , GRCh38.p12 chr7|NT_187653.1: 143,455-152,878 LINC03014
    esv2660593copy number variation56estd199human GRCh37 chrX: 91,610,345-91,620,792 , GRCh38.p12 chrX: 92,355,346-92,365,793 PCDH11X
    esv2672284copy number variation80estd199human GRCh37 chr11: 107,233,995-107,244,392 , GRCh38.p12 chr11: 107,363,269-107,373,666 CWF19L2
    esv2671979copy number variation4estd199human GRCh37 chr16: 80,903,476-80,913,830 , GRCh38.p12 chr16: 80,869,579-80,879,933 ARLNC1
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2658229copy number variation46estd199human GRCh37 chr3: 125,712,244-125,722,069 , GRCh38.p12 chr3: 125,993,401-126,003,226 ALG1L1P
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