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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935410copy number variation1nstd209human GRCh38 chr17: 67,731,238-67,731,513 , GRCh37.p13 chr17: 65,727,354-65,727,629 NOL11
    nsv5729577mobile element insertion1nstd211human GRCh38 chr17: 67,722,041-67,722,041 , GRCh37.p13 chr17: 65,718,157-65,718,157 NOL11
    nsv5705724mobile element insertion2nstd211human GRCh38 chr17: 67,735,582-67,735,582 , GRCh37.p13 chr17: 65,731,698-65,731,698 NOL11
    nsv5593855copy number variation1nstd207human GRCh38 chr17: 67,731,238-67,731,513 , GRCh37.p13 chr17: 65,727,354-65,727,629 NOL11
    nsv5562126mobile element insertion1nstd206human GRCh38 chr17: 67,722,041-67,722,092 , GRCh37.p13 chr17: 65,718,157-65,718,208 NOL11
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5528900copy number variation1nstd206human GRCh38 chr17: 67,714,406-67,717,355 , GRCh37.p13 chr17: 65,710,522-65,713,471 NOL11, LOC101928045
    nsv5520749copy number variation1nstd206human GRCh38 chr17: 67,731,255-67,731,514 , GRCh37.p13 chr17: 65,727,371-65,727,630 NOL11
    nsv5519647copy number variation1nstd206human GRCh38 chr17: 67,727,544-67,727,995 , GRCh37.p13 chr17: 65,723,660-65,724,111 NOL11
    nsv5430960mobile element insertion1nstd206human GRCh38 chr17: 67,735,582-67,735,633 , GRCh37.p13 chr17: 65,731,698-65,731,749 NOL11
    nsv5384706mobile element deletion2nstd186human GRCh37 chr17: 65,727,371-65,727,630 , GRCh38.p12 chr17: 67,731,255-67,731,514 NOL11
    nsv5299631copy number variation1nstd204human GRCh38.p13 chr17: 67,712,075-67,717,953 , GRCh37.p13 chr17: 65,708,191-65,714,069 NOL11, LOC101928045
    nsv5289880copy number variation1nstd204human GRCh37.p13 chr17: 65,727,417-65,936,105 , GRCh38.p13 chr17: 67,731,301-68,072,300 BPTF, KPNA2, 7 more genes
    nsv5212165mobile element deletion1nstd204human GRCh38.p13 chr17: 67,731,255-67,731,514 , GRCh37.p13 chr17: 65,727,371-65,727,630 NOL11
    nsv5187304mobile element insertion1nstd203human GRCh38 chr17: 67,721,260-67,721,267 , GRCh37.p13 chr17: 65,717,376-65,717,383 NOL11
    nsv5146630mobile element insertion1nstd203human GRCh38 chr17: 67,735,565-67,735,582 , GRCh37.p13 chr17: 65,731,681-65,731,698 NOL11
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5010747copy number variation1nstd200human GRCh38 chr17: 67,724,899-67,728,042 , GRCh37.p13 chr17: 65,721,015-65,724,158 NOL11
    nsv5010746copy number variation1nstd200human GRCh38 chr17: 67,714,406-67,717,355 , GRCh37.p13 chr17: 65,710,522-65,713,471 LOC101928045, NOL11
    nsv4907365mobile element deletion1nstd200human GRCh38 chr17: 67,731,255-67,731,514 , GRCh37.p13 chr17: 65,727,371-65,727,630 NOL11
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