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Items: 1 to 20 of 3517

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3834770copy number variation743estd219human GRCh37 chr4: 34,781,317-34,849,886 , GRCh38.p12 chr4|NW_003315915.1: 272,024-340,593 , GRCh38.p12 chr4: 34,779,695-34,848,264 LOC105378262
    esv3853507copy number variation1095estd219human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3834769copy number variation743estd219human GRCh37 chr4: 34,779,933-34,828,997 , GRCh38.p12 chr4|NW_003315915.1: 270,640-319,704 , GRCh38.p12 chr4: 34,778,311-34,827,375 LOC105378262
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3821789copy number variation1062estd219human GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810 CFHR3
    esv3871990copy number variation8estd219human GRCh37 chr13: 110,732,474-110,761,471 , GRCh38.p12 chr13: 110,080,127-110,109,124 RN7SL783P
    esv3851668copy number variation544estd219human GRCh37 chr7: 141,765,307-141,792,849 , GRCh38.p12 chr7|NT_187562.1: 27,387-54,929 , GRCh38.p12 chr7: 142,065,507-142,093,049 MGAM
    esv3871992copy number variation8estd219human GRCh37 chr13: 110,740,960-110,763,627 , GRCh38.p12 chr13: 110,088,613-110,111,280 RN7SL783P
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3860443copy number variation1029estd219human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3852311copy number variation601estd219human GRCh37 chr8: 2,250,517-2,266,603 , GRCh38.p12 chr8|NT_187576.1: 485,727-501,813 LOC105377783
    esv3879060copy number variation208estd219human GRCh37 chr17: 15,042,705-15,059,719 , GRCh38.p12 chr17: 15,139,388-15,156,402 LOC107984976
    esv3833727copy number variation624estd219human GRCh37 chr3: 195,456,936-195,471,412 , GRCh38.p12 chr3|NT_187688.1: 50,160-64,603 , GRCh38.p12 chr3|NT_187689.1: 100,562-115,038 , GRCh38.p12 chr3|NT_187690.1: 50,159-64,610 , GRCh38.p12 chr3|NT_187691.1: 50,266-64,780 , GRCh38.p12 chr3|NT_187532.1: 100,562-115,038 , GRCh38.p12 chr3: 195,730,065-195,744,541 , GRCh38.p12 chr3|NT_187678.1: 51,460-65,948 , GRCh38.p12 chr3|NT_187649.1: 50,164-64,603 MUC20
    esv3851465copy number variation1169estd219human GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
    esv3890498copy number variation1565estd219human GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709 TMLHE
    esv3830293copy number variation263estd219human GRCh37 chr3: 53,026,796-53,039,244 , GRCh38.p12 chr3: 52,992,780-53,005,228 SFMBT1
    esv3848096copy number variation146estd219human GRCh37 chr7: 6,129,998-6,141,944 , GRCh38.p12 chr7: 6,090,367-6,102,313 USP42
    esv3865462copy number variation1142estd219human GRCh37 chr11: 107,234,989-107,247,884 , GRCh38.p12 chr11: 107,364,263-107,377,158 CWF19L2
    esv3853510copy number variation1096estd219human GRCh37 chr8: 39,310,276-39,322,581 , GRCh38.p12 chr8: 39,452,757-39,465,062 ADAM3A
    esv3852446copy number variation3estd219human GRCh37 chr8: 4,475,821-4,486,175 , GRCh38.p12 chr8: 4,618,299-4,628,653 CSMD1
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