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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918040copy number variation1nstd209human GRCh38 chr11: 73,881,491-73,885,343 , GRCh37.p13 chr11: 73,592,536-73,596,388 PAAF1
    nsv5915239copy number variation1nstd209human GRCh38 chr11: 73,898,170-73,898,220 , GRCh37.p13 chr11: 73,609,215-73,609,265 PAAF1
    nsv5851162copy number variation1nstd209human GRCh38 chr11: 73,881,347-73,885,565 , GRCh37.p13 chr11: 73,592,392-73,596,610 PAAF1
    nsv5722548mobile element insertion1nstd211human GRCh38 chr11: 73,891,436-73,891,436 , GRCh37.p13 chr11: 73,602,481-73,602,481 PAAF1
    nsv5698086mobile element insertion1nstd211human GRCh38 chr11: 73,918,378-73,918,378 , GRCh37.p13 chr11: 73,629,423-73,629,423 PAAF1
    nsv5655330insertion1nstd207human GRCh38 chr11: 73,897,370-73,897,370 , GRCh37.p13 chr11: 73,608,415-73,608,415 PAAF1
    nsv5601502copy number variation1nstd207human GRCh38 chr11: 73,896,833-73,897,011 , GRCh37.p13 chr11: 73,607,878-73,608,056 PAAF1
    nsv5597396copy number variation1nstd207human GRCh38 chr11: 73,897,026-73,897,103 , GRCh37.p13 chr11: 73,608,071-73,608,148 PAAF1
    nsv5544576insertion1nstd206human GRCh38 chr11: 73,897,370-73,897,370 , GRCh37.p13 chr11: 73,608,415-73,608,415 PAAF1
    nsv5511572copy number variation1nstd206human GRCh38 chr11: 73,868,389-73,908,934 , GRCh37.p13 chr11: 73,579,434-73,619,979 COA4, PAAF1
    nsv5509061copy number variation1nstd206human GRCh38 chr11: 73,881,517-73,885,334 , GRCh37.p13 chr11: 73,592,562-73,596,379 PAAF1
    nsv5507382copy number variation1nstd206human GRCh38 chr11: 73,924,269-73,924,944 , GRCh37.p13 chr11: 73,635,314-73,635,989 PAAF1
    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
    nsv5308944copy number variation1nstd204human GRCh38.p13 chr11: 73,901,651-73,904,063 , GRCh37.p13 chr11: 73,612,696-73,615,108 PAAF1
    nsv5128198mobile element insertion1nstd203human GRCh38 chr11: 73,904,778-73,904,797 , GRCh37.p13 chr11: 73,615,823-73,615,842 PAAF1
    nsv4989052copy number variation1nstd200human GRCh38 chr11: 73,868,341-73,908,961 , GRCh37.p13 chr11: 73,579,386-73,620,006 COA4, PAAF1
    nsv4987293copy number variation1nstd200human GRCh38 chr11: 73,913,963-73,920,410 , GRCh37.p13 chr11: 73,625,008-73,631,455 PAAF1, ARPC3P4
    nsv4987292copy number variation1nstd200human GRCh38 chr11: 73,899,554-73,901,964 , GRCh37.p13 chr11: 73,610,599-73,613,009 PAAF1
    nsv4987291copy number variation1nstd200human GRCh38 chr11: 73,882,680-73,885,161 , GRCh37.p13 chr11: 73,593,725-73,596,206 PAAF1
    nsv4987290copy number variation1nstd200human GRCh38 chr11: 73,881,542-73,885,330 , GRCh37.p13 chr11: 73,592,587-73,596,375 PAAF1
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