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Items: 1 to 20 of 904

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075211inversion1nstd229human GRCh38 chr9: 19,274,357-19,287,111 , GRCh37.p13 chr9: 19,274,355-19,287,109 DENND4C
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7065086inversion1nstd229human GRCh38 chr9: 19,326,297-19,326,308 , GRCh37.p13 chr9: 19,326,295-19,326,306 DENND4C
    nsv7063743inversion1nstd229human GRCh38 chr9: 19,172,900-19,248,428 , GRCh37.p13 chr9: 19,172,898-19,248,426 RPS6P10, DENND4C
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv7060715inversion1nstd229human GRCh38 chr9: 19,315,002-19,315,768 , GRCh37.p13 chr9: 19,315,000-19,315,766 DENND4C
    nsv7060215inversion1nstd229human GRCh38 chr9: 19,315,156-19,315,770 , GRCh37.p13 chr9: 19,315,154-19,315,768 DENND4C
    nsv7059107inversion1nstd229human GRCh38 chr9: 19,193,470-19,250,206 , GRCh37.p13 chr9: 19,193,468-19,250,204 RPS6P10, DENND4C
    nsv6877883copy number variation1nstd229human GRCh38 chr9: 19,315,801-19,503,700 , GRCh37.p13 chr9: 19,315,799-19,503,698 RPS6, ACER2, 4 more genes
    nsv6877415copy number variation1nstd229human GRCh38 chr9: 18,863,175-19,659,789 , GRCh37.p13 chr9: 18,863,173-19,659,787 ACER2, ADAMTSL1, 15 more genes
    nsv6876319copy number variation1nstd229human GRCh38 chr9: 19,292,308-19,302,036 , GRCh37.p13 chr9: 19,292,306-19,302,034 DENND4C
    nsv6876237copy number variation1nstd229human GRCh38 chr9: 19,262,601-19,520,400 , GRCh37.p13 chr9: 19,262,599-19,520,398 NDUFA5P3, SLC24A2, 5 more genes
    nsv6875931copy number variation1nstd229human GRCh38 chr9: 19,341,543-19,353,597 , GRCh37.p13 chr9: 19,341,541-19,353,595 DENND4C
    nsv6875852copy number variation1nstd229human GRCh38 chr9: 19,260,601-19,265,200 , GRCh37.p13 chr9: 19,260,599-19,265,198 DENND4C
    nsv6875614copy number variation1nstd229human GRCh38 chr9: 19,235,773-19,402,755 , GRCh37.p13 chr9: 19,235,771-19,402,753 NDUFA5P3, DENND4C, 1 more genes
    nsv6875467copy number variation1nstd229human GRCh38 chr9: 19,235,255-19,235,520 , GRCh37.p13 chr9: 19,235,253-19,235,518 DENND4C
    nsv6875264copy number variation1nstd229human GRCh38 chr9: 19,373,501-19,375,800 , GRCh37.p13 chr9: 19,373,499-19,375,798 RPS6, DENND4C
    nsv6874525copy number variation1nstd229human GRCh38 chr9: 19,220,818-19,357,470 , GRCh37.p13 chr9: 19,220,816-19,357,468 DENND4C
    nsv6874497copy number variation1nstd229human GRCh38 chr9: 19,168,613-19,533,503 , GRCh37.p13 chr9: 19,168,611-19,533,501 ACER2, RPS6, 6 more genes
    nsv6874370copy number variation1nstd229human GRCh38 chr9: 19,077,797-19,550,661 , GRCh37.p13 chr9: 19,077,795-19,550,659 RPS6P10, MAP1LC3BP1, 8 more genes
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