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Items: 1 to 20 of 433

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128479insertion1nstd186human GRCh37 chr2: 101,493,889-101,493,889 , GRCh38.p12 chr2: 100,877,427-100,877,427 NPAS2
    nsv5883879copy number variation1nstd209human GRCh38 chr2: 100,822,927-100,842,198 , GRCh37.p13 chr2: 101,439,389-101,458,660 NPAS2
    nsv5875816copy number variation1nstd209human GRCh38 chr2: 100,953,023-100,953,201 , GRCh37.p13 chr2: 101,569,485-101,569,663 NPAS2
    nsv5830870copy number variation1nstd209human GRCh38 chr2: 100,822,879-100,839,728 , GRCh37.p13 chr2: 101,439,341-101,456,190 NPAS2
    nsv5689499mobile element insertion1nstd211human GRCh38 chr2: 100,861,975-100,861,975 , GRCh37.p13 chr2: 101,478,437-101,478,437 NPAS2
    nsv5572963copy number variation1nstd207human GRCh38 chr2: 100,953,023-100,953,201 , GRCh37.p13 chr2: 101,569,485-101,569,663 NPAS2
    nsv5563482sequence alteration1nstd206human GRCh38 chr2: 100,760,576-100,882,484 , GRCh37.p13 chr2: 101,377,038-101,498,946 NPAS2
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5538333insertion1nstd206human GRCh38 chr2: 100,877,427-100,877,427 , GRCh37.p13 chr2: 101,493,889-101,493,889 NPAS2
    nsv5453806copy number variation1nstd206human GRCh38 chr2: 100,953,026-100,953,202 , GRCh37.p13 chr2: 101,569,488-101,569,664 NPAS2
    nsv5446746copy number variation1nstd206human GRCh38 chr2: 100,889,478-100,892,939 , GRCh37.p13 chr2: 101,505,940-101,509,401 NPAS2
    nsv5434930copy number variation1nstd206human GRCh38 chr2: 100,885,742-100,888,131 , GRCh37.p13 chr2: 101,502,204-101,504,593 NPAS2
    nsv5434164copy number variation1nstd206human GRCh38 chr2: 100,951,976-100,952,146 , GRCh37.p13 chr2: 101,568,438-101,568,608 NPAS2
    nsv5411717mobile element insertion1nstd206human GRCh38 chr2: 100,861,975-100,862,026 , GRCh37.p13 chr2: 101,478,437-101,478,488 NPAS2
    nsv5383630copy number variation2nstd186human GRCh37 chr2: 101,569,488-101,569,664 , GRCh38.p12 chr2: 100,953,026-100,953,202 NPAS2
    nsv5360940translocation1nstd200human GRCh38 chr2: 100,952,308-100,952,308 , GRCh38 chr2: 100,936,793-100,936,793 , GRCh37.p13 chr2: 101,553,255-101,553,255 , GRCh37.p13 chr2: 101,568,770-101,568,770 NPAS2
    nsv5360939translocation1nstd200human GRCh38 chr2: 100,936,469-100,936,469 , GRCh38 chr2: 100,936,523-100,936,523 , GRCh37.p13 chr2: 101,552,931-101,552,931 , GRCh37.p13 chr2: 101,552,985-101,552,985 NPAS2
    nsv5360938translocation1nstd200human GRCh38 chr2: 100,926,628-100,926,628 , GRCh38 chr2: 100,927,787-100,927,787 , GRCh37.p13 chr2: 101,544,249-101,544,249 , GRCh37.p13 chr2: 101,543,090-101,543,090 NPAS2
    nsv5360937translocation1nstd200human GRCh38 chr2: 100,880,922-100,880,922 , GRCh38 chr2: 100,880,855-100,880,855 , GRCh37.p13 chr2: 101,497,317-101,497,317 , GRCh37.p13 chr2: 101,497,384-101,497,384 NPAS2
    nsv5340769translocation1nstd200human GRCh37 chr2: 101,543,090-101,543,090 , GRCh37 chr2: 101,544,249-101,544,249 , GRCh38.p12 chr2: 100,927,787-100,927,787 , GRCh38.p12 chr2: 100,926,628-100,926,628 NPAS2
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