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Items: 1 to 20 of 737

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124666insertion1nstd186human GRCh37 chrX: 10,478,570-10,478,570 , GRCh38.p12 chrX: 10,510,530-10,510,530 MID1
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5980432copy number variation2nstd102humanPathogenic, Likely benign GRCh37 chrX: 8,501,036-11,318,732 , GRCh38.p12 chrX: 8,532,995-11,300,612 FAM9A, NOLC1P1, 23 more genes
    nsv5976210copy number variation1nstd209human GRCh38 chrX: 10,560,842-10,563,015 , GRCh37.p13 chrX: 10,528,882-10,531,055 MID1
    nsv5975114copy number variation2nstd209human GRCh38 chrX: 10,726,672-10,731,673 , GRCh37.p13 chrX: 10,694,712-10,699,713 MID1
    nsv5970704copy number variation1nstd209human GRCh38 chrX: 10,717,453-10,719,884 , GRCh37.p13 chrX: 10,685,493-10,687,924 MID1
    nsv5968329copy number variation1nstd209human GRCh38 chrX: 10,708,712-10,730,723 , GRCh37.p13 chrX: 10,676,752-10,698,763 MID1
    nsv5887552copy number variation1nstd209human GRCh38 chrX: 10,560,820-10,563,040 , GRCh37.p13 chrX: 10,528,860-10,531,080 MID1
    nsv5887130copy number variation1nstd209human GRCh38 chrX: 10,727,630-10,733,054 , GRCh37.p13 chrX: 10,695,670-10,701,094 MID1
    nsv5885069copy number variation1nstd209human GRCh38 chrX: 10,484,697-10,484,788 , GRCh37.p13 chrX: 10,452,737-10,452,828 MID1
    nsv5884027copy number variation1nstd209human GRCh38 chrX: 10,713,583-10,730,828 , GRCh37.p13 chrX: 10,681,623-10,698,868 MID1
    nsv5881699copy number variation1nstd209human GRCh38 chrX: 10,799,749-10,799,819 , GRCh37.p13 chrX: 10,817,868-10,817,938 MID1
    nsv5879622copy number variation1nstd209human GRCh38 chrX: 10,454,293-10,454,351 , GRCh37.p13 chrX: 10,422,333-10,422,391 MID1
    nsv5879542copy number variation1nstd209human GRCh38 chrX: 10,585,248-10,590,332 , GRCh37.p13 chrX: 10,553,288-10,558,372 MID1
    nsv5870777copy number variation1nstd209human GRCh38 chrX: 10,589,434-10,589,549 , GRCh37.p13 chrX: 10,557,474-10,557,589 MID1
    nsv5727498mobile element insertion2nstd211human GRCh38 chrX: 10,603,055-10,603,055 , GRCh37.p13 chrX: 10,571,095-10,571,095 MID1
    nsv5727213mobile element insertion1nstd211human GRCh38 chrX: 10,452,209-10,452,209 , GRCh37.p13 chrX: 10,420,249-10,420,249 MID1
    nsv5726922mobile element insertion1nstd211human GRCh38 chrX: 10,683,800-10,683,800 , GRCh37.p13 chrX: 10,651,840-10,651,840 MID1
    nsv5721005mobile element insertion1nstd211human GRCh38 chrX: 10,787,545-10,787,545 , GRCh37.p13 chrX: 10,805,664-10,805,664 MID1
    nsv5720433mobile element insertion1nstd211human GRCh38 chrX: 10,745,693-10,745,693 , GRCh37.p13 chrX: 10,713,733-10,713,733 MID1
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