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Items: 1 to 20 of 2739

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3621845copy number variation340estd214human GRCh37 chr9: 132,654,988-132,798,900 , GRCh38.p12 chr9: 129,892,709-130,036,621 FNBP1
    esv3641565copy number variation196estd214human GRCh37 chr18: 2,659,472-2,734,289 , GRCh38.p12 chr18: 2,659,473-2,734,291 SMCHD1
    esv3600181copy number variation743estd214human GRCh37 chr4: 34,781,317-34,849,886 , GRCh38.p12 chr4: 34,779,695-34,848,264 , GRCh38.p12 chr4|NW_003315915.1: 272,024-340,593 LOC105378262
    esv3616948copy number variation1095estd214human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3600180copy number variation743estd214human 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
    esv3587491copy number variation2473estd214human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3816878copy number variation26estd214human GRCh37 chrX: 80,748,583-80,780,550 , GRCh38.p12 chrX: 81,493,084-81,525,051 LOC105373285
    esv3632214copy number variation1037estd214human GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443 MTCO2P3
    esv3600875copy number variation1672estd214human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3615267copy number variation544estd214human GRCh37 chr7: 141,765,307-141,792,849 , GRCh38.p12 chr7: 142,065,507-142,093,049 , GRCh38.p12 chr7|NT_187562.1: 27,387-54,929 MGAM
    esv3620473copy number variation1254estd214human GRCh37 chr9: 43,580,844-43,606,160 , GRCh38.p12 chr9: 42,208,229-42,233,545 LOC112268036
    esv3597711copy number variation73estd214human GRCh37 chr3: 128,378,657-128,404,290 , GRCh38.p12 chr3: 128,659,814-128,685,447 POU5F1P6
    esv3591709copy number variation1476estd214human GRCh37 chr2: 98,136,216-98,156,567 , GRCh38.p12 chr2: 97,519,753-97,540,104 ANKRD36B
    esv3587880copy number variation879estd214human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3628470copy number variation4908estd214human GRCh37 chr12: 8,568,920-8,587,027 , GRCh38.p12 chr12: 8,416,324-8,434,431 OR7E148P
    esv3593502copy number variation1244estd214human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3620460copy number variation1877estd214human GRCh37 chr9: 41,971,191-41,985,717 , GRCh38.p12 chr9: 39,826,173-39,840,699 FGF7P3
    esv3644676copy number variation1486estd214human GRCh37 chr19: 52,134,835-52,149,093 , GRCh38.p12 chr19: 51,631,582-51,645,840 SIGLEC14
    esv3599249copy number variation624estd214human GRCh37 chr3: 195,456,936-195,471,412 , GRCh38.p12 chr3|NT_187689.1: 100,562-115,038 , GRCh38.p12 chr3|NT_187532.1: 100,562-115,038 , GRCh38.p12 chr3|NT_187649.1: 50,164-64,603 , GRCh38.p12 chr3|NT_187690.1: 50,159-64,610 , GRCh38.p12 chr3|NT_187691.1: 50,266-64,780 , GRCh38.p12 chr3|NT_187688.1: 50,160-64,603 , GRCh38.p12 chr3: 195,730,065-195,744,541 , GRCh38.p12 chr3|NT_187678.1: 51,460-65,948 MUC20
    esv3612768copy number variation3estd214human GRCh37 chr7: 33,503,377-33,518,858 , GRCh38.p12 chr7: 33,463,765-33,479,246 BBS9
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