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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966592insertion1nstd209human GRCh38 chr3: 179,874,737-179,874,737 , GRCh37.p13 chr3: 179,592,525-179,592,525 PEX5L
    nsv5956941insertion1nstd209human GRCh38 chr3: 179,917,039-179,917,039 , GRCh37.p13 chr3: 179,634,827-179,634,827 PEX5L, PEX5L-AS2
    nsv5950949insertion1nstd209human GRCh38 chr3: 180,010,266-180,010,266 , GRCh37.p13 chr3: 179,728,054-179,728,054 PEX5L
    nsv5899811copy number variation1nstd209human GRCh38 chr3: 179,962,014-179,962,069 , GRCh37.p13 chr3: 179,679,802-179,679,857 PEX5L
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5894604copy number variation1nstd209human GRCh38 chr3: 179,936,551-179,937,015 , GRCh37.p13 chr3: 179,654,339-179,654,803 PEX5L
    nsv5724852mobile element insertion2nstd211human GRCh38 chr3: 179,823,286-179,823,286 , GRCh37.p13 chr3: 179,541,074-179,541,074 PEX5L
    nsv5690179mobile element insertion2nstd211human GRCh38 chr3: 180,000,660-180,000,660 , GRCh37.p13 chr3: 179,718,448-179,718,448 PEX5L
    nsv5681964mobile element insertion2nstd211human GRCh38 chr3: 179,917,054-179,917,054 , GRCh37.p13 chr3: 179,634,842-179,634,842 PEX5L-AS2, PEX5L
    nsv5620569insertion1nstd207human GRCh38 chr3: 179,823,285-179,823,285 , GRCh37.p13 chr3: 179,541,073-179,541,073 PEX5L
    nsv5618241insertion1nstd207human GRCh38 chr3: 179,962,014-179,962,014 , GRCh37.p13 chr3: 179,679,802-179,679,802 PEX5L
    nsv5614281insertion1nstd207human GRCh38 chr3: 179,917,039-179,917,039 , GRCh37.p13 chr3: 179,634,827-179,634,827 PEX5L, PEX5L-AS2
    nsv5579106copy number variation1nstd207human GRCh38 chr3: 180,023,792-180,023,842 , GRCh37.p13 chr3: 179,741,580-179,741,630 PEX5L
    nsv5575737copy number variation1nstd207human GRCh38 chr3: 179,901,187-179,901,238 , GRCh37.p13 chr3: 179,618,975-179,619,026 PEX5L, PEX5L-AS2
    nsv5571610copy number variation1nstd207human GRCh38 chr3: 179,936,551-179,937,015 , GRCh37.p13 chr3: 179,654,339-179,654,803 PEX5L
    nsv5540146insertion1nstd206human GRCh38 chr3: 180,000,660-180,000,696 , GRCh37.p13 chr3: 179,718,448-179,718,484 PEX5L
    nsv5535675insertion1nstd206human GRCh38 chr3: 179,859,549-179,859,549 , GRCh37.p13 chr3: 179,577,337-179,577,337 PEX5L
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5449512copy number variation1nstd206human GRCh38 chr3: 179,805,299-179,806,199 , GRCh37.p13 chr3: 179,523,087-179,523,987 PEX5L
    nsv5448619copy number variation1nstd206human GRCh38 chr3: 179,858,559-179,859,549 , GRCh37.p13 chr3: 179,576,347-179,577,337 PEX5L
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