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Items: 1 to 20 of 1303

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3988779copy number variation6estd229human GRCh37 chr4: 49,588,812-49,628,667 , GRCh38.p12 chr4: 49,586,795-49,626,650 SNX18P25
    esv3983565copy number variation2estd229human GRCh37 chr9: 44,431,651-44,470,350 , GRCh38.p12 chr9: 42,500,769-42,539,468 CNTNAP3P8
    esv3988066copy number variation22estd229human GRCh37 chr20: 1,561,051-1,593,900 , GRCh38.p12 chr20: 1,580,405-1,613,254 SIRPB1
    esv3985262copy number variation10estd229human GRCh37 chr13: 112,932,901-112,965,300 , GRCh38.p12 chr13: 112,278,587-112,310,986 , GRCh38.p12 chr13|NT_187592.1: 95,705-119,790 LINC01043
    esv3982442copy number variation7estd229human GRCh37 chr7: 64,593,451-64,620,900 , GRCh38.p12 chr7: 65,133,073-65,160,522 INTS4P1
    esv3989607copy number variation5estd229human GRCh37 chr2: 98,136,451-98,162,100 , GRCh38.p12 chr2: 97,519,988-97,545,637 ANKRD36B
    esv3989440copy number variation4estd229human GRCh37 chr2: 74,013,751-74,035,350 , GRCh38.p12 chr2: 73,786,624-73,808,223 C2orf78
    esv3983077copy number variation5estd229human GRCh37 chr8: 75,311,101-75,330,000 , GRCh38.p12 chr8: 74,398,866-74,417,765 GDAP1
    esv3988828copy number variation5estd229human GRCh37 chr2: 203,295,601-203,312,700 , GRCh38.p12 chr2: 202,430,878-202,447,977 BMPR2
    esv3977415copy number variation1estd229human GRCh37 chr3: 24,891,301-24,908,400 , GRCh38.p12 chr3: 24,849,810-24,866,909 RARB
    esv3981853copy number variation2estd229human GRCh37 chr7: 10,788,301-10,802,700 , GRCh38.p12 chr7: 10,748,674-10,763,073 MGC4859
    esv3985060copy number variation12estd229human GRCh37 chr1: 2,608,873-2,622,712 , GRCh38.p12 chr1: 2,677,434-2,691,273 TTC34
    esv3983626copy number variation1estd229human GRCh37 chr9: 514,351-527,850 , GRCh38.p12 chr9: 514,351-527,850 KANK1
    esv3988633copy number variation15estd229human GRCh37 chr2: 1,527,941-1,541,250 , GRCh38.p12 chr2: 1,524,169-1,537,478 , GRCh38.p12 chr2|NT_187529.1: 206,540-219,849 TPO
    esv3986828copy number variation3estd229human GRCh37 chr16: 78,371,551-78,384,600 , GRCh38.p12 chr16: 78,337,654-78,350,703 WWOX
    esv3976549copy number variation3estd229human GRCh37 chr5: 155,475,901-155,488,950 , GRCh38.p12 chr5: 156,048,891-156,061,940 SGCD
    esv3982813copy number variation2estd229human GRCh37 chr3: 87,889,951-87,902,550 , GRCh38.p12 chr3: 87,840,801-87,853,400 HTR1F
    esv3989554copy number variation4estd229human GRCh37 chr1: 111,376,801-111,388,500 , GRCh38.p12 chr1: 110,834,179-110,845,878 NRBF2P3
    esv3987521copy number variation2estd229human GRCh37 chr18: 66,745,351-66,757,050 , GRCh38.p12 chr18: 69,078,114-69,089,813 CCDC102B
    esv3980371copy number variation4estd229human GRCh37 chr5: 70,327,351-70,339,050 , GRCh38.p12 chr5: 71,031,524-71,043,223 GTF2H2
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