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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    esv3644983copy number variation2409estd214human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3600875copy number variation1672estd214human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3623922copy number variation1739estd214human GRCh37 chr10: 81,474,561-81,502,396 , GRCh38.p12 chr10: 79,714,805-79,742,640 NUTM2B-AS1
    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
    esv3622528copy number variation1estd214human GRCh37 chr10: 19,511,771-19,538,902 , GRCh38.p12 chr10: 19,222,842-19,249,973 MALRD1
    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
    esv3620460copy number variation1877estd214human GRCh37 chr9: 41,971,191-41,985,717 , GRCh38.p12 chr9: 39,826,173-39,840,699 FGF7P3
    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
    esv3624344copy number variation716estd214human GRCh37 chr10: 100,688,139-100,702,531 , GRCh38.p12 chr10: 98,928,382-98,942,774 HPSE2
    esv3607277copy number variation424estd214human GRCh37 chr5: 155,475,886-155,488,649 , GRCh38.p12 chr5: 156,048,876-156,061,639 SGCD
    esv3816876copy number variation1565estd214human GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709 TMLHE
    esv3636945copy number variation1210estd214human GRCh37 chr15: 76,884,546-76,895,794 , GRCh38.p12 chr15: 76,592,205-76,603,453 SCAPER
    esv3587155copy number variation2179estd214human GRCh37 chr1: 110,230,075-110,241,247 , GRCh38.p12 chr1: 109,687,453-109,698,625 GSTM1
    esv3591108copy number variation103estd214human GRCh37 chr2: 66,185,959-66,197,058 , GRCh38.p12 chr2: 65,958,825-65,969,924 LINC02934
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