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Items: 1 to 20 of 3863

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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
    esv3858757copy number variation1estd219human GRCh37 chr9: 119,615,692-119,698,370 , GRCh38.p12 chr9: 116,853,413-116,936,091 ASTN2
    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
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3878813copy number variation73estd219human GRCh37 chr17: 6,100,426-6,134,511 , GRCh38.p12 chr17: 6,197,106-6,231,191 RNU6-1264P
    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
    esv3872467copy number variation1estd219human GRCh37 chr14: 33,653,339-33,678,560 , GRCh38.p12 chr14: 33,184,133-33,209,354 NPAS3
    esv3856296copy number variation62estd219human GRCh37 chr9: 5,383,925-5,404,804 , GRCh38.p12 chr9: 5,383,925-5,404,804 PLGRKT
    esv3848975copy number variation54estd219human GRCh37 chr7: 34,895,675-34,913,807 , GRCh38.p12 chr7: 34,856,063-34,874,195 NPSR1
    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
    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
    esv3859331copy number variation1estd219human GRCh37 chr10: 2,035,987-2,047,506 , GRCh38.p12 chr10: 1,993,793-2,005,312 LINC00700
    esv3831054copy number variation2estd219human GRCh37 chr3: 86,176,631-86,189,105 , GRCh38.p12 chr3: 86,127,481-86,139,955 LOC102723364
    esv3865462copy number variation1142estd219human GRCh37 chr11: 107,234,989-107,247,884 , GRCh38.p12 chr11: 107,364,263-107,377,158 CWF19L2
    esv3827269copy number variation329estd219human GRCh37 chr2: 180,410,908-180,422,736 , GRCh38.p12 chr2: 179,546,181-179,558,009 ZNF385B
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