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Items: 1 to 20 of 4027

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3820479copy number variation1estd219human GRCh37 chr1: 113,810,961-113,933,784 , GRCh38.p12 chr1: 113,268,339-113,391,162 MAGI3
    esv3820541copy number variation1estd219human GRCh37 chr1: 116,321,097-116,377,526 , GRCh38.p12 chr1: 115,778,476-115,834,905 NHLH2
    esv3830173copy number variation520estd219human GRCh37 chr3: 46,803,577-46,851,159 , GRCh38.p12 chr3: 46,762,087-46,809,669 PRSS44P
    esv3869509copy number variation2estd219human GRCh37 chr12: 133,494,602-133,537,098 , GRCh38.p12 chr12: 132,918,016-132,960,512 ZNF605
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3820496copy number variation1estd219human GRCh37 chr1: 114,482,901-114,515,484 , GRCh38.p12 chr1: 113,940,279-113,972,862 HIPK1
    esv3825301copy number variation15estd219human GRCh37 chr2: 98,856,216-98,886,613 , GRCh38.p12 chr2: 98,239,753-98,270,150 VWA3B
    esv3820507copy number variation1estd219human GRCh37 chr1: 114,939,198-114,968,568 , GRCh38.p12 chr1: 114,396,576-114,425,946 TRIM33
    esv3821789copy number variation1062estd219human GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810 CFHR3
    esv3820512copy number variation1estd219human GRCh37 chr1: 115,130,092-115,157,074 , GRCh38.p12 chr1: 114,587,471-114,614,453 DENND2C
    esv3857199copy number variation26estd219human GRCh37 chr9: 28,738,986-28,767,444 , GRCh38.p12 chr9: 28,738,988-28,767,446 LINGO2
    esv3842790copy number variation95estd219human GRCh37 chr5: 155,566,445-155,591,598 , GRCh38.p12 chr5: 156,139,435-156,164,588 SGCD
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3837478copy number variation71estd219human GRCh37 chr4: 144,904,824-144,923,549 , GRCh38.p12 chr4: 143,983,671-144,002,396 GYPB
    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
    esv3842791copy number variation93estd219human GRCh37 chr5: 155,577,187-155,591,410 , GRCh38.p12 chr5: 156,150,177-156,164,400 SGCD
    esv3861771copy number variation716estd219human GRCh37 chr10: 100,688,139-100,702,531 , GRCh38.p12 chr10: 98,928,382-98,942,774 HPSE2
    esv3843269copy number variation52estd219human GRCh37 chr5: 177,309,116-177,322,865 , GRCh38.p12 chr5|NT_187546.1: 16,651-30,400 , GRCh38.p12 chr5|NT_187652.1: 16,651-30,400 , GRCh38.p12 chr5: 177,882,115-177,895,864 LOC728554
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