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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7098415copy number variation1nstd102humanPathogenic GRCh37 chrX: 43,515,590-44,970,656 , GRCh38.p12 chrX: 43,656,342-45,111,411 RPSAP61, RPL19P20, 16 more genes
    nsv7098314copy number variation2nstd102humanPathogenic GRCh37 chrX: 43,515,590-43,817,891 , GRCh38.p12 chrX: 43,656,342-43,958,645 NDP, MAOA, 2 more genes
    nsv7087524copy number variation1nstd229human GRCh38 chrX: 43,865,212-43,887,177 , GRCh37.p13 chrX: 43,724,458-43,746,423 MAOB
    nsv7087523copy number variation1nstd229human GRCh38 chrX: 43,859,382-43,875,792 , GRCh37.p13 chrX: 43,718,628-43,735,038 MAOB
    nsv7087522copy number variation1nstd229human GRCh38 chrX: 43,844,474-43,850,110 , GRCh37.p13 chrX: 43,703,720-43,709,356 MAOB
    nsv7087521copy number variation1nstd229human GRCh38 chrX: 43,844,415-43,848,669 , GRCh37.p13 chrX: 43,703,661-43,707,915 MAOB
    nsv7087520copy number variation1nstd229human GRCh38 chrX: 43,822,414-43,827,859 , GRCh37.p13 chrX: 43,681,661-43,687,105 MAOB
    nsv7087519copy number variation1nstd229human GRCh38 chrX: 43,818,631-43,951,183 , GRCh37.p13 chrX: 43,677,878-43,810,429 MAOB, NDP, 1 more genes
    nsv7087518copy number variation1nstd229human GRCh38 chrX: 43,815,835-43,816,435 , GRCh37.p13 chrX: 43,675,082-43,675,682 MAOB
    nsv7087517copy number variation1nstd229human GRCh38 chrX: 43,809,961-43,810,268 , GRCh37.p13 chrX: 43,669,208-43,669,515 MAOB
    nsv7087516copy number variation1nstd229human GRCh38 chrX: 43,791,208-43,804,945 , GRCh37.p13 chrX: 43,650,455-43,664,192 MAOB
    nsv7087515copy number variation1nstd229human GRCh38 chrX: 43,785,096-43,787,015 , GRCh37.p13 chrX: 43,644,343-43,646,262 MAOB
    nsv7087514copy number variation1nstd229human GRCh38 chrX: 43,783,221-43,788,826 , GRCh37.p13 chrX: 43,642,468-43,648,073 MAOB
    nsv7087513copy number variation1nstd229human GRCh38 chrX: 43,777,701-44,141,600 , GRCh37.p13 chrX: 43,636,948-44,000,846 MAOB, NDP, 2 more genes
    nsv7087512copy number variation1nstd229human GRCh38 chrX: 43,752,597-43,833,765 , GRCh37.p13 chrX: 43,611,844-43,693,011 MAOB
    nsv7087502copy number variation1nstd229human GRCh38 chrX: 43,595,421-44,016,474 , GRCh37.p13 chrX: 43,454,669-43,875,720 MAOA, NDP, 2 more genes
    nsv7087497copy number variation1nstd229human GRCh38 chrX: 43,528,401-43,767,158 , GRCh37.p13 chrX: 43,387,649-43,626,405 MAOA, MAOB
    nsv7037928inversion1nstd229human GRCh38 chrX: 43,833,613-43,833,740 , GRCh37.p13 chrX: 43,692,859-43,692,986 MAOB
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