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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
    esv2673642copy number variation50estd199human GRCh37 chrX: 91,853,345-91,909,992 , GRCh38.p12 chrX: 92,598,346-92,654,993 PCDH11X
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    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
    esv2678880copy number variation28estd199human GRCh37 chr13: 25,160,669-25,177,071 , GRCh38.p12 chr13: 24,586,531-24,602,933 TPTE2P6
    esv2664362copy number variation25estd199human GRCh37 chr8: 2,251,326-2,267,068 , GRCh38.p12 chr8|NT_187576.1: 486,536-502,278 LOC105377783
    esv2675775copy number variation27estd199human GRCh37 chr9: 514,141-527,931 , GRCh38.p12 chr9: 514,141-527,931 KANK1
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2664238copy number variation1estd199human GRCh37 chr4: 54,069,338-54,081,957 , GRCh38.p12 chr4: 53,203,171-53,215,790 SCFD2
    esv2658204copy number variation8estd199human GRCh37 chr3: 87,889,775-87,902,357 , GRCh38.p12 chr3: 87,840,625-87,853,207 HTR1F
    esv2668652copy number variation25estd199human GRCh37 chr1: 111,377,295-111,389,642 , GRCh38.p12 chr1: 110,834,673-110,847,020 NRBF2P3
    esv2665413copy number variation30estd199human GRCh37 chr8: 63,214,945-63,226,892 , GRCh38.p12 chr8: 62,302,386-62,314,333 NKAIN3
    esv2670295copy number variation118estd199human GRCh37 chr3: 114,656,952-114,668,601 , GRCh38.p12 chr3: 114,938,105-114,949,754 ZBTB20
    esv2670043copy number variation1estd199human GRCh37 chr1: 99,191,778-99,202,922 , GRCh38.p12 chr1: 98,726,222-98,737,366 SNX7
    esv2666369copy number variation2estd199human GRCh37 chr2: 130,544,848-130,555,544 , GRCh38.p12 chr2: 129,787,275-129,797,971 LOC107985945
    esv2660593copy number variation56estd199human GRCh37 chrX: 91,610,345-91,620,792 , GRCh38.p12 chrX: 92,355,346-92,365,793 PCDH11X
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