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Items: 1 to 20 of 262

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5721195mobile element insertion1nstd211human GRCh38 chr2: 98,798,438-98,798,438 , GRCh37.p13 chr2: 99,414,901-99,414,901 CRACDL
    nsv5686437mobile element insertion1nstd211human GRCh38 chr2: 98,916,647-98,916,647 , GRCh37.p13 chr2: 99,533,110-99,533,110 CRACDL
    nsv5624339insertion1nstd207human GRCh38 chr2: 98,930,326-98,930,326 , GRCh37.p13 chr2: 99,546,789-99,546,789 CRACDL
    nsv5621457insertion1nstd207human GRCh38 chr2: 98,795,073-98,795,073 , GRCh37.p13 chr2: 99,411,536-99,411,536 CRACDL
    nsv5620206insertion1nstd207human GRCh38 chr2: 98,900,122-98,900,122 , GRCh37.p13 chr2: 99,516,585-99,516,585 CRACDL
    nsv5613527insertion1nstd207human GRCh38 chr2: 98,930,348-98,930,348 , GRCh37.p13 chr2: 99,546,811-99,546,811 CRACDL
    nsv5559056sequence alteration1nstd206human GRCh38 chr2: 98,866,541-98,866,545 , GRCh37.p13 chr2: 99,483,004-99,483,008 CRACDL
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5541150insertion1nstd206human GRCh38 chr2: 98,866,541-98,866,541 , GRCh37.p13 chr2: 99,483,004-99,483,004 CRACDL
    nsv5453439copy number variation1nstd206human GRCh38 chr2: 98,869,405-98,869,459 , GRCh37.p13 chr2: 99,485,868-99,485,922 CRACDL
    nsv5447733copy number variation1nstd206human GRCh38 chr2: 98,808,497-98,808,610 , GRCh37.p13 chr2: 99,424,960-99,425,073 CRACDL
    nsv5445361copy number variation1nstd206human GRCh38 chr2: 98,886,444-98,892,529 , GRCh37.p13 chr2: 99,502,907-99,508,992 CRACDL
    nsv5411083mobile element insertion1nstd206human GRCh38 chr2: 98,916,647-98,916,698 , GRCh37.p13 chr2: 99,533,110-99,533,161 CRACDL
    nsv5206993mobile element deletion1nstd204human GRCh38.p13 chr2: 98,904,958-98,905,273 , GRCh37.p13 chr2: 99,521,421-99,521,736 CRACDL
    nsv5066371mobile element insertion1nstd203human GRCh38 chr2: 98,916,631-98,916,647 , GRCh37.p13 chr2: 99,533,094-99,533,110 CRACDL
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908245copy number variation1nstd200human GRCh38 chr2: 98,874,982-98,877,984 , GRCh37.p13 chr2: 99,491,445-99,494,447 CRACDL
    nsv4908244copy number variation1nstd200human GRCh38 chr2: 98,862,444-98,863,609 , GRCh37.p13 chr2: 99,478,907-99,480,072 CRACDL
    nsv4908243copy number variation1nstd200human GRCh38 chr2: 98,812,979-98,813,170 , GRCh37.p13 chr2: 99,429,442-99,429,633 CRACDL
    nsv4908242copy number variation1nstd200human GRCh38 chr2: 98,789,500-98,792,261 , GRCh37.p13 chr2: 99,405,963-99,408,724 CRACDL
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