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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3886598copy number variation1estd219human GRCh37 chr21: 32,221,068-32,303,033 , GRCh38.p12 chr21: 30,848,749-30,930,714 KRTAP11-1
    esv3841222copy number variation49estd219human GRCh37 chr5: 97,050,505-97,128,253 , GRCh38.p12 chr5: 97,714,801-97,792,549 LOC391813
    esv3841223copy number variation40estd219human GRCh37 chr5: 97,049,822-97,126,058 , GRCh38.p12 chr5: 97,714,118-97,790,354 LOC391813
    esv3872670copy number variation646estd219human GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445 LINC02315
    esv3853507copy number variation1095estd219human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3841221copy number variation54estd219human GRCh37 chr5: 97,047,859-97,096,156 , GRCh38.p12 chr5: 97,712,155-97,760,452 LOC391813
    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
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3848556copy number variation2estd219human GRCh37 chr7: 17,509,206-17,530,791 , GRCh38.p12 chr7: 17,469,582-17,491,167 LINC02889
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3827261copy number variation1244estd219human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3833727copy number variation624estd219human GRCh37 chr3: 195,456,936-195,471,412 , GRCh38.p12 chr3|NT_187688.1: 50,160-64,603 , GRCh38.p12 chr3|NT_187689.1: 100,562-115,038 , GRCh38.p12 chr3|NT_187690.1: 50,159-64,610 , GRCh38.p12 chr3|NT_187691.1: 50,266-64,780 , GRCh38.p12 chr3|NT_187532.1: 100,562-115,038 , GRCh38.p12 chr3: 195,730,065-195,744,541 , GRCh38.p12 chr3|NT_187678.1: 51,460-65,948 , GRCh38.p12 chr3|NT_187649.1: 50,164-64,603 MUC20
    esv3851465copy number variation1169estd219human GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
    esv3878137copy number variation1122estd219human GRCh37 chr16: 78,371,328-78,385,326 , GRCh38.p12 chr16: 78,337,431-78,351,429 WWOX
    esv3842787copy number variation424estd219human GRCh37 chr5: 155,475,886-155,488,649 , GRCh38.p12 chr5: 156,048,876-156,061,639 SGCD
    esv3830293copy number variation263estd219human GRCh37 chr3: 53,026,796-53,039,244 , GRCh38.p12 chr3: 52,992,780-53,005,228 SFMBT1
    esv3822089copy number variation99estd219human GRCh37 chr1: 213,001,037-213,014,756 , GRCh38.p12 chr1: 212,827,695-212,841,414 SPATA45
    esv3875253copy number variation292estd219human GRCh37 chr15: 56,789,510-56,801,390 , GRCh38.p12 chr15: 56,497,312-56,509,192
    esv3873919copy number variation7estd219human GRCh37 chr14: 91,255,997-91,267,383 , GRCh38.p12 chr14: 90,789,653-90,801,039 TTC7B
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