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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3860960copy number variation2estd219human GRCh37 chr10: 68,160,377-68,517,719 , GRCh38.p12 chr10: 66,400,619-66,757,961 CTNNA3
    esv3860964copy number variation3estd219human GRCh37 chr10: 68,170,435-68,402,820 , GRCh38.p12 chr10: 66,410,677-66,643,062 CTNNA3
    esv3860990copy number variation7estd219human GRCh37 chr10: 68,319,822-68,410,658 , GRCh38.p12 chr10: 66,560,064-66,650,900 CTNNA3
    esv3857122copy number variation3estd219human GRCh37 chr9: 26,707,649-26,788,041 , GRCh38.p12 chr9: 26,707,651-26,788,043 LOC105376000
    esv3860987copy number variation10estd219human GRCh37 chr10: 68,296,963-68,377,290 , GRCh38.p12 chr10: 66,537,205-66,617,532 CTNNA3
    esv3860978copy number variation5estd219human GRCh37 chr10: 68,249,228-68,328,058 , GRCh38.p12 chr10: 66,489,470-66,568,300 CTNNA3
    esv3861006copy number variation2estd219human GRCh37 chr10: 68,450,803-68,514,314 , GRCh38.p12 chr10: 66,691,045-66,754,556 CTNNA3
    esv3860971copy number variation5estd219human GRCh37 chr10: 68,229,169-68,290,523 , GRCh38.p12 chr10: 66,469,411-66,530,765 CTNNA3
    esv3860965copy number variation3estd219human GRCh37 chr10: 68,183,928-68,244,775 , GRCh38.p12 chr10: 66,424,170-66,485,017 CTNNA3
    esv3860976copy number variation6estd219human GRCh37 chr10: 68,247,697-68,301,600 , GRCh38.p12 chr10: 66,487,939-66,541,842 CTNNA3
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3860993copy number variation13estd219human GRCh37 chr10: 68,328,040-68,362,312 , GRCh38.p12 chr10: 66,568,282-66,602,554 CTNNA3
    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
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3860998copy number variation14estd219human GRCh37 chr10: 68,339,593-68,367,025 , GRCh38.p12 chr10: 66,579,835-66,607,267 CTNNA3
    esv3861002copy number variation3estd219human GRCh37 chr10: 68,424,363-68,449,653 , GRCh38.p12 chr10: 66,664,605-66,689,895 CTNNA3
    esv3861003copy number variation3estd219human GRCh37 chr10: 68,425,832-68,448,692 , GRCh38.p12 chr10: 66,666,074-66,688,934 CTNNA3
    esv3860988copy number variation8estd219human GRCh37 chr10: 68,298,614-68,320,479 , GRCh38.p12 chr10: 66,538,856-66,560,721 CTNNA3
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
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