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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
    nsv7089522copy number variation1nstd229human GRCh38 chrX: 81,176,853-81,188,430 , GRCh37.p13 chrX: 80,432,352-80,443,929 HMGN5
    nsv7089521copy number variation1nstd229human GRCh38 chrX: 81,174,620-81,182,286 , GRCh37.p13 chrX: 80,430,119-80,437,785 HMGN5
    nsv7089520copy number variation1nstd229human GRCh38 chrX: 81,170,101-81,174,100 , GRCh37.p13 chrX: 80,425,600-80,429,599 HMGN5
    nsv7089519copy number variation1nstd229human GRCh38 chrX: 81,160,851-81,161,608 , GRCh37.p13 chrX: 80,416,350-80,417,107 HMGN5
    nsv7089518copy number variation1nstd229human GRCh38 chrX: 81,157,801-81,159,800 , GRCh37.p13 chrX: 80,413,300-80,415,299 HMGN5
    nsv7089517copy number variation1nstd229human GRCh38 chrX: 81,156,073-81,226,956 , GRCh37.p13 chrX: 80,411,572-80,482,455 HMGN5, SH3BGRL
    nsv7089516copy number variation1nstd229human GRCh38 chrX: 81,151,731-81,155,180 , GRCh37.p13 chrX: 80,407,230-80,410,679 HMGN5
    nsv7089515copy number variation1nstd229human GRCh38 chrX: 81,140,912-81,149,129 , GRCh37.p13 chrX: 80,396,411-80,404,628 HMGN5
    nsv7089514copy number variation1nstd229human GRCh38 chrX: 81,126,825-81,133,324 , GRCh37.p13 chrX: 80,382,324-80,388,823 HMGN5
    nsv7089513copy number variation1nstd229human GRCh38 chrX: 81,125,639-81,129,698 , GRCh37.p13 chrX: 80,381,138-80,385,197 HMGN5
    nsv7089512copy number variation1nstd229human GRCh38 chrX: 81,125,370-81,132,399 , GRCh37.p13 chrX: 80,380,869-80,387,898 HMGN5
    nsv7089509copy number variation1nstd229human GRCh38 chrX: 81,065,154-81,153,176 , GRCh37.p13 chrX: 80,320,653-80,408,675 HMGN5
    nsv7089507copy number variation1nstd229human GRCh38 chrX: 81,045,335-81,839,994 , GRCh37.p13 chrX: 80,300,834-81,095,493 LOC105373284, LOC105373285, 4 more genes
    nsv7089457copy number variation1nstd229human GRCh38 chrX: 80,508,685-81,495,723 , GRCh37.p13 chrX: 79,764,184-80,751,222 LOC105373284, WBP11P3, 11 more genes
    nsv7034748inversion1nstd229human GRCh38 chrX: 80,442,808-84,464,579 , GRCh37.p13 chrX: 79,698,307-83,719,587 EIF3MP1, HDX, 28 more genes
    nsv7027401inversion1nstd229human GRCh38 chrX: 81,187,655-81,203,113 , GRCh37.p13 chrX: 80,443,154-80,458,612 SH3BGRL, HMGN5
    nsv6636960copy number variation1nstd102humanUncertain significance GRCh37 chrX: 80,404,540-81,278,950 , GRCh38.p12 chrX: 81,149,041-82,023,501 HMGN5, SH3BGRL, 5 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
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