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Items: 1 to 20 of 3754

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3863622copy number variation1estd219human GRCh37 chr11: 38,853,392-38,961,880 , GRCh38.p12 chr11: 38,831,842-38,940,330 LOC101928563
    esv3834770copy number variation743estd219human GRCh37 chr4: 34,781,317-34,849,886 , GRCh38.p12 chr4|NW_003315915.1: 272,024-340,593 , GRCh38.p12 chr4: 34,779,695-34,848,264 LOC105378262
    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
    esv3834769copy number variation743estd219human 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
    esv3830173copy number variation520estd219human GRCh37 chr3: 46,803,577-46,851,159 , GRCh38.p12 chr3: 46,762,087-46,809,669 PRSS44P
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3878175copy number variation3estd219human GRCh37 chr16: 79,252,675-79,293,584 , GRCh38.p12 chr16: 79,218,778-79,259,687 MAF
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3870498copy number variation1037estd219human GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443 MTCO2P3
    esv3870904copy number variation198estd219human GRCh37 chr13: 69,244,390-69,269,055 , GRCh38.p12 chr13: 68,670,258-68,694,923 RN7SL761P
    esv3878178copy number variation1estd219human GRCh37 chr16: 79,275,166-79,294,062 , GRCh38.p12 chr16: 79,241,269-79,260,165 MAF
    esv3860443copy number variation1029estd219human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3827261copy number variation1244estd219human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3861771copy number variation716estd219human GRCh37 chr10: 100,688,139-100,702,531 , GRCh38.p12 chr10: 98,928,382-98,942,774 HPSE2
    esv3842787copy number variation424estd219human GRCh37 chr5: 155,475,886-155,488,649 , GRCh38.p12 chr5: 156,048,876-156,061,639 SGCD
    esv3843269copy number variation52estd219human GRCh37 chr5: 177,309,116-177,322,865 , GRCh38.p12 chr5|NT_187546.1: 16,651-30,400 , GRCh38.p12 chr5|NT_187652.1: 16,651-30,400 , GRCh38.p12 chr5: 177,882,115-177,895,864 LOC728554
    esv3844934copy number variation25estd219human GRCh37 chr6: 58,301,698-58,314,469 , GRCh38.p12 chr6: 57,975,420-57,988,191 LOC101927293
    esv3820413copy number variation357estd219human GRCh37 chr1: 111,376,500-111,388,793 , GRCh38.p12 chr1: 110,833,878-110,846,171 NRBF2P3
    esv3832158copy number variation15estd219human GRCh37 chr3: 133,014,921-133,028,615 , GRCh38.p12 chr3: 133,296,077-133,309,771 TMEM108
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