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Items: 1 to 20 of 728

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146231copy number variation1nstd232human GRCh37.p13 chrX: 19,485,812-19,485,873 , GRCh38.p12 chrX: 19,467,694-19,467,755 MAP3K15
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098359copy number variation1nstd102humanUncertain significance GRCh37 chrX: 18,525,053-20,284,750 , GRCh38.p12 chrX: 18,506,933-20,266,632 PPEF1, PDHA1, 23 more genes
    nsv7098012copy number variation1nstd102humanUncertain significance GRCh37 chrX: 19,368,035-19,377,771 , GRCh38.p12 chrX: 19,349,917-19,359,653 PDHA1, MAP3K15
    nsv7086084copy number variation1nstd229human GRCh38 chrX: 19,494,816-19,497,243 , GRCh37.p13 chrX: 19,512,934-19,515,361 MAP3K15, EIF5P2
    nsv7086083copy number variation1nstd229human GRCh38 chrX: 19,490,153-19,490,186 , GRCh37.p13 chrX: 19,508,271-19,508,304 MAP3K15
    nsv7086082copy number variation1nstd229human GRCh38 chrX: 19,489,501-19,492,000 , GRCh37.p13 chrX: 19,507,619-19,510,118 MAP3K15
    nsv7086081copy number variation1nstd229human GRCh38 chrX: 19,483,433-19,579,275 , GRCh37.p13 chrX: 19,501,551-19,597,393 SH3KBP1, EIF5P2, 1 more genes
    nsv7086080copy number variation1nstd229human GRCh38 chrX: 19,476,001-19,485,900 , GRCh37.p13 chrX: 19,494,119-19,504,018 MAP3K15
    nsv7086079copy number variation1nstd229human GRCh38 chrX: 19,474,651-19,481,631 , GRCh37.p13 chrX: 19,492,769-19,499,749 MAP3K15
    nsv7086078copy number variation1nstd229human GRCh38 chrX: 19,473,407-19,475,558 , GRCh37.p13 chrX: 19,491,525-19,493,676 MAP3K15
    nsv7086077copy number variation1nstd229human GRCh38 chrX: 19,466,564-19,586,918 , GRCh37.p13 chrX: 19,484,682-19,605,036 MAP3K15, SH3KBP1, 1 more genes
    nsv7086076copy number variation1nstd229human GRCh38 chrX: 19,449,194-19,449,716 , GRCh37.p13 chrX: 19,467,312-19,467,834 MAP3K15
    nsv7086075copy number variation1nstd229human GRCh38 chrX: 19,449,001-19,452,700 , GRCh37.p13 chrX: 19,467,119-19,470,818 MAP3K15
    nsv7086074copy number variation1nstd229human GRCh38 chrX: 19,448,708-19,449,308 , GRCh37.p13 chrX: 19,466,826-19,467,426 MAP3K15
    nsv7086073copy number variation1nstd229human GRCh38 chrX: 19,447,701-19,453,400 , GRCh37.p13 chrX: 19,465,819-19,471,518 MAP3K15
    nsv7086072copy number variation1nstd229human GRCh38 chrX: 19,447,201-19,449,700 , GRCh37.p13 chrX: 19,465,319-19,467,818 MAP3K15
    nsv7086071copy number variation1nstd229human GRCh38 chrX: 19,443,721-19,445,750 , GRCh37.p13 chrX: 19,461,839-19,463,868 MAP3K15
    nsv7086070copy number variation1nstd229human GRCh38 chrX: 19,439,431-19,574,805 , GRCh37.p13 chrX: 19,457,549-19,592,923 MAP3K15, SH3KBP1, 1 more genes
    nsv7086069copy number variation1nstd229human GRCh38 chrX: 19,437,430-19,437,647 , GRCh37.p13 chrX: 19,455,548-19,455,765 MAP3K15
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