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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980140insertion1nstd209human GRCh38 chr11: 72,073,048-72,073,048 , GRCh37.p13 chr11: 71,784,094-71,784,094 NUMA1
    nsv5979966insertion1nstd209human GRCh38 chr11: 72,049,583-72,049,583 , GRCh37.p13 chr11: 71,760,629-71,760,629 NUMA1
    nsv5721739mobile element insertion1nstd211human GRCh38 chr11: 72,074,754-72,074,754 , GRCh37.p13 chr11: 71,785,800-71,785,800 NUMA1
    nsv5716278mobile element insertion1nstd211human GRCh38 chr11: 72,053,841-72,053,841 , GRCh37.p13 chr11: 71,764,887-71,764,887 NUMA1
    nsv5695638mobile element insertion2nstd211human GRCh38 chr11: 72,026,660-72,026,660 , GRCh37.p13 chr11: 71,737,706-71,737,706 NUMA1
    nsv5561134mobile element insertion1nstd206human GRCh38 chr11: 72,053,855-72,053,892 , GRCh37.p13 chr11: 71,764,901-71,764,938 NUMA1
    nsv5398763mobile element insertion1nstd206human GRCh38 chr11: 72,026,660-72,026,711 , GRCh37.p13 chr11: 71,737,706-71,737,757 NUMA1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5373706translocation1nstd200human GRCh38 chr11: 72,000,616-72,000,616 , GRCh38 chr11: 72,001,332-72,001,332 , GRCh37.p13 chr11: 71,711,662-71,711,662 , GRCh37.p13 chr11: 71,712,378-71,712,378 NUMA1, IL18BP
    nsv5373705translocation1nstd200human GRCh38 chr11: 72,000,336-72,000,336 , GRCh38 chr11: 72,001,335-72,001,335 , GRCh37.p13 chr11: 71,711,382-71,711,382 , GRCh37.p13 chr11: 71,712,381-71,712,381 IL18BP, NUMA1
    nsv5343157translocation1nstd200human GRCh37 chr11: 71,712,378-71,712,378 , GRCh37 chr11: 71,711,662-71,711,662 , GRCh38.p12 chr11: 72,000,616-72,000,616 , GRCh38.p12 chr11: 72,001,332-72,001,332 IL18BP, NUMA1
    nsv5329732translocation1nstd200human GRCh37 chr11: 71,712,381-71,712,381 , GRCh37 chr11: 71,711,382-71,711,382 , GRCh38.p12 chr11: 72,000,336-72,000,336 , GRCh38.p12 chr11: 72,001,335-72,001,335 NUMA1, IL18BP
    nsv5278677copy number variation1nstd204human GRCh37.p13 chr11: 71,772,747-71,889,344 , GRCh38.p13 chr11: 72,061,701-72,178,300 FOLR3, NUMA1, 7 more genes
    nsv5187596mobile element insertion1nstd203human GRCh38 chr11: 72,053,841-72,053,841 , GRCh37.p13 chr11: 71,764,887-71,764,887 NUMA1
    nsv5184970mobile element insertion1nstd203human GRCh38 chr11: 72,038,161-72,038,176 , GRCh37.p13 chr11: 71,749,207-71,749,222 NUMA1
    nsv5130714mobile element insertion1nstd203human GRCh38 chr11: 72,026,651-72,026,660 , GRCh37.p13 chr11: 71,737,697-71,737,706 NUMA1
    nsv5127712mobile element insertion1nstd203human GRCh38 chr11: 72,011,625-72,011,640 , GRCh37.p13 chr11: 71,722,671-71,722,686 NUMA1
    nsv5121082mobile element insertion1nstd203human GRCh38 chr11: 72,064,275-72,064,275 , GRCh37.p13 chr11: 71,775,321-71,775,321 NUMA1
    nsv4987246copy number variation1nstd200human GRCh38 chr11: 72,068,712-72,078,792 , GRCh37.p13 chr11: 71,779,758-71,789,838 MIR3165, LRTOMT, 1 more genes
    nsv4980106copy number variation1nstd200human GRCh38 chr11: 72,044,699-72,050,327 , GRCh37.p13 chr11: 71,755,745-71,761,373 NUMA1
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