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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918173copy number variation1nstd209human GRCh38 chr10: 1,160,725-1,160,781 , GRCh37.p13 chr10: 1,206,665-1,206,721 LINC00200
    nsv5914956copy number variation1nstd209human GRCh38 chr10: 1,163,458-1,163,541 , GRCh37.p13 chr10: 1,209,398-1,209,481 LINC00200
    nsv5912942copy number variation1nstd209human GRCh38 chr10: 1,159,708-1,159,851 , GRCh37.p13 chr10: 1,205,648-1,205,791 LINC00200, LOC105376344
    nsv5910177copy number variation1nstd209human GRCh38 chr10: 1,159,638-1,159,779 , GRCh37.p13 chr10: 1,205,578-1,205,719 LINC00200, LOC105376344
    nsv5729531mobile element insertion2nstd211human GRCh38 chr10: 1,160,182-1,160,182 , GRCh37.p13 chr10: 1,206,122-1,206,122 LINC00200
    nsv5672604copy number variation1nstd102humanPathogenic GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038 PITRM1-AS1, TRV-TAC3-1, 133 more genes
    nsv5639688insertion2nstd207human GRCh38 chr10: 1,163,542-1,163,542 , GRCh37.p13 chr10: 1,209,482-1,209,482 LINC00200
    nsv5635842insertion1nstd207human GRCh38 chr10: 1,159,829-1,159,829 , GRCh37.p13 chr10: 1,205,769-1,205,769 LINC00200, LOC105376344
    nsv5562633mobile element insertion1nstd206human GRCh38 chr10: 1,160,182-1,160,233 , GRCh37.p13 chr10: 1,206,122-1,206,173 LINC00200
    nsv5303975copy number variation1nstd204human GRCh38.p13 chr10: 1,033,801-2,011,873 , GRCh37.p13 chr10: 1,079,741-2,054,067 LINC00200, LOC105376342, 9 more genes
    nsv5183426mobile element insertion1nstd203human GRCh38 chr10: 1,160,168-1,160,182 , GRCh37.p13 chr10: 1,206,108-1,206,122 LINC00200
    nsv4973476copy number variation1nstd200human GRCh38 chr10: 1,143,149-1,249,515 , GRCh37.p13 chr10: 1,189,089-1,291,567 ADARB2, LINC00200, 1 more genes
    nsv4973475copy number variation1nstd200human GRCh38 chr10: 1,126,317-1,175,181 , GRCh37.p13 chr10: 1,172,257-1,221,121 LOC105376344, WDR37, 1 more genes
    nsv4847790copy number variation1nstd200human GRCh37 chr10: 1,079,751-2,054,058 , GRCh38.p12 chr10: 1,033,811-2,011,864 LOC105376342, IDI2-AS1, 9 more genes
    nsv4844126copy number variation1nstd200human GRCh37 chr10: 1,189,089-1,291,567 , GRCh38.p12 chr10: 1,143,149-1,249,515 LOC105376344, LINC00200, 1 more genes
    nsv4759641insertion1nstd199human GRCh37 chr10: 1,205,652-1,205,652 , GRCh38.p12 chr10: 1,159,712-1,159,712 LINC00200, LOC105376344
    nsv4750722insertion1nstd199human GRCh37 chr10: 1,209,406-1,209,406 , GRCh38.p12 chr10: 1,163,466-1,163,466 LINC00200
    nsv4748436copy number variation1nstd199human GRCh37 chr10: 1,210,595-1,210,716 , GRCh38.p12 chr10: 1,164,655-1,164,776 LINC00200
    nsv4728832copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-1,281,266 , GRCh38.p12 chr10: 54,086-1,235,330 DDX20P1, ZMYND11, 20 more genes
    nsv4675836copy number variation1nstd102humanUncertain significance GRCh37 chr10: 970,276-1,236,463 , GRCh38.p12 chr10: 924,336-1,190,523 LARP4B-DT, IDI2, 8 more genes
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