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Items: 1 to 20 of 2594

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3634197copy number variation646estd214human GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445 LINC02315
    esv3616948copy number variation1095estd214human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    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
    esv3588471copy number variation1062estd214human GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810 CFHR3
    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
    esv3591709copy number variation1476estd214human GRCh37 chr2: 98,136,216-98,156,567 , GRCh38.p12 chr2: 97,519,753-97,540,104 ANKRD36B
    esv3591756copy number variation5estd214human GRCh37 chr2: 101,215,395-101,233,723 , GRCh38.p12 chr2: 100,598,933-100,617,261 LINC01849
    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
    esv3609614copy number variation648estd214human GRCh37 chr6: 77,437,459-77,453,275 , GRCh38.p12 chr6: 76,727,742-76,743,558 LOC105377861
    esv3816114copy number variation9estd214human GRCh37 chrX: 95,275,725-95,291,165 , GRCh38.p12 chrX: 96,020,726-96,036,166 RN7SL379P
    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
    esv3611756copy number variation518estd214human GRCh37 chr7: 151,255-160,130 , GRCh38.p12 chr7|NT_187558.1: 107,060-119,474 , GRCh38.p12 chr7|NT_187653.1: 143,576-152,451 , GRCh38.p12 chr7: 151,255-160,130 LINC03014
    esv3646598copy number variation610estd214human GRCh37 chr21: 23,653,294-23,667,590 , GRCh38.p12 chr21: 22,280,974-22,295,270 , GRCh38.p12 chr21|NW_003315968.2: 185,203-199,499 LOC107985508
    esv3816876copy number variation1565estd214human GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709 TMLHE
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