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Items: 1 to 20 of 3218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3875848copy number variation139estd219human GRCh37 chr15: 86,064,810-86,182,627 , GRCh38.p12 chr15: 85,521,579-85,639,396 AKAP13
    esv3872670copy number variation646estd219human GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445 LINC02315
    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
    esv3870498copy number variation1037estd219human GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443 MTCO2P3
    esv3821789copy number variation1062estd219human GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810 CFHR3
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3877198copy number variation52estd219human GRCh37 chr16: 29,556,778-29,578,806 , GRCh38.p12 chr16: 29,545,457-29,567,485 SMG1P2
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3834975copy number variation1estd219human GRCh37 chr4: 42,476,539-42,493,596 , GRCh38.p12 chr4: 42,474,522-42,491,579 ATP8A1
    esv3830348copy number variation90estd219human GRCh37 chr3: 56,610,335-56,626,937 , GRCh38.p12 chr3: 56,576,307-56,592,909 CCDC66
    esv3830347copy number variation130estd219human GRCh37 chr3: 56,607,734-56,621,640 , GRCh38.p12 chr3: 56,573,706-56,587,612 CCDC66
    esv3851465copy number variation1169estd219human GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
    esv3864936copy number variation232estd219human GRCh37 chr11: 89,798,932-89,810,560 , GRCh38.p12 chr11: 90,065,764-90,077,392 TRIM49C
    esv3850412copy number variation193estd219human GRCh37 chr7: 91,030,693-91,042,943 , GRCh38.p12 chr7: 91,401,378-91,413,628 LINC02932
    esv3818888copy number variation539estd219human GRCh37 chr1: 35,101,427-35,111,985 , GRCh38.p12 chr1: 34,635,826-34,646,384 LOC105378641
    esv3834976copy number variation1estd219human GRCh37 chr4: 42,481,453-42,492,822 , GRCh38.p12 chr4: 42,479,436-42,490,805 ATP8A1
    esv3833638copy number variation2212estd219human GRCh37 chr3: 192,875,179-192,885,555 , GRCh38.p12 chr3: 193,157,390-193,167,766 VEZF1P1
    esv3881073copy number variation235estd219human GRCh37 chr18: 14,450,647-14,460,558 , GRCh38.p12 chr18: 14,450,648-14,460,559 LONRF2P1
    esv3845520copy number variation388estd219human GRCh37 chr6: 81,283,720-81,293,577 , GRCh38.p12 chr6: 80,574,003-80,583,860 LOC112267962
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