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Items: 1 to 20 of 357

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147464copy number variation1nstd232human GRCh37.p13 chrX: 47,100,047-47,100,171 , GRCh38.p12 chrX: 47,240,648-47,240,772 USP11
    nsv7146642copy number variation1nstd232human GRCh37.p13 chrX: 47,093,162-47,093,214 , GRCh38.p12 chrX: 47,233,763-47,233,815 USP11
    nsv7146214copy number variation1nstd232human GRCh37.p13 chrX: 47,100,847-47,100,936 , GRCh38.p12 chrX: 47,241,448-47,241,537 USP11
    nsv7145399copy number variation1nstd232human GRCh37.p13 chrX: 47,101,920-47,102,022 , GRCh38.p12 chrX: 47,242,521-47,242,623 USP11
    nsv7144955copy number variation1nstd232human GRCh37.p13 chrX: 47,101,703-47,101,834 , GRCh38.p12 chrX: 47,242,304-47,242,435 USP11
    nsv7144272copy number variation1nstd232human GRCh37.p13 chrX: 47,107,096-47,107,188 , GRCh38.p12 chrX: 47,247,697-47,247,789 USP11
    nsv7144067insertion1nstd232human GRCh37.p13 chrX: 47,103,000-47,103,000 , GRCh38.p12 chrX: 47,243,601-47,243,601 USP11
    nsv7143658copy number variation1nstd232human GRCh37.p13 chrX: 47,104,322-47,104,412 , GRCh38.p12 chrX: 47,244,923-47,245,013 USP11
    nsv7141746copy number variation1nstd232human GRCh37.p13 chrX: 47,106,619-47,106,700 , GRCh38.p12 chrX: 47,247,220-47,247,301 USP11
    nsv7137329insertion1nstd232human GRCh37.p13 chrX: 47,099,307-47,099,307 , GRCh38.p12 chrX: 47,239,908-47,239,908 USP11
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098786copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-51,241,672 , GRCh38.p12 chrX: 46,606,952-51,498,820 LOC100419232, LOC791091, 172 more genes
    nsv7098533copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-47,489,243 , GRCh38.p12 chrX: 46,606,952-47,629,844 MIR4769, RP2, 32 more genes
    nsv7098417copy number variation2nstd102humanPathogenic GRCh37 chrX: 46,618,120-48,549,553 , GRCh38.p12 chrX: 46,758,685-48,691,162 ZNF81, LOC105373194, 84 more genes
    nsv7098318copy number variation3nstd102humanUncertain significance GRCh37 chrX: 47,001,716-50,659,607 , GRCh38.p12 chrX: 47,142,317-50,916,607 PYY3, CCDC120, 148 more genes
    nsv7098317copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-50,659,607 , GRCh38.p12 chrX: 46,606,952-50,916,607 PLP2, RN7SL262P, 160 more genes
    nsv7087818copy number variation1nstd229human GRCh38 chrX: 47,246,726-47,246,794 , GRCh37.p13 chrX: 47,106,125-47,106,193 USP11
    nsv7087817copy number variation1nstd229human GRCh38 chrX: 47,245,567-47,245,772 , GRCh37.p13 chrX: 47,104,966-47,105,171 USP11
    nsv7087816copy number variation1nstd229human GRCh38 chrX: 47,214,801-47,240,400 , GRCh37.p13 chrX: 47,079,811-47,099,799 CDK16, UBA1, 2 more genes
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