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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123863copy number variation1nstd186human GRCh37 chr17: 2,398,873-2,402,729 , GRCh38.p12 chr17: 2,495,579-2,499,435 METTL16
    nsv6112772copy number variation1nstd102humanPathogenic GRCh37 chr17: 2,313,096-3,735,525 , GRCh38.p12 chr17: 2,409,802-3,832,231 LOC105371592, OR3A5P, 49 more genes
    nsv5971809insertion1nstd209human GRCh38 chr17: 2,417,058-2,417,058 , GRCh37.p13 chr17: 2,320,352-2,320,352 METTL16
    nsv5946695copy number variation1nstd209human GRCh38 chr17: 2,491,669-2,495,489 , GRCh37.p13 chr17: 2,394,963-2,398,783 METTL16
    nsv5944818copy number variation1nstd209human GRCh38 chr17: 2,495,605-2,499,440 , GRCh37.p13 chr17: 2,398,899-2,402,734 METTL16
    nsv5942824copy number variation1nstd209human GRCh38 chr17: 2,444,986-2,445,119 , GRCh37.p13 chr17: 2,348,280-2,348,413 METTL16
    nsv5938629copy number variation1nstd209human GRCh38 chr17: 2,492,105-2,494,891 , GRCh37.p13 chr17: 2,395,399-2,398,185 METTL16
    nsv5932061copy number variation1nstd209human GRCh38 chr17: 2,435,652-2,435,755 , GRCh37.p13 chr17: 2,338,946-2,339,049 METTL16
    nsv5881319copy number variation1nstd209human GRCh38 chr17: 2,492,901-2,495,255 , GRCh37.p13 chr17: 2,396,195-2,398,549 METTL16
    nsv5881234copy number variation1nstd209human GRCh38 chr17: 2,491,957-2,495,155 , GRCh37.p13 chr17: 2,395,251-2,398,449 METTL16
    nsv5880098copy number variation1nstd209human GRCh38 chr17: 2,495,781-2,499,158 , GRCh37.p13 chr17: 2,399,075-2,402,452 METTL16
    nsv5875865copy number variation1nstd209human GRCh38 chr17: 2,478,399-2,479,423 , GRCh37.p13 chr17: 2,381,693-2,382,717 METTL16
    nsv5871934copy number variation1nstd209human GRCh38 chr17: 2,481,324-2,483,523 , GRCh37.p13 chr17: 2,384,618-2,386,817 METTL16
    nsv5718797mobile element insertion2nstd211human GRCh38 chr17: 2,448,800-2,448,800 , GRCh37.p13 chr17: 2,352,094-2,352,094 METTL16
    nsv5657290insertion1nstd207human GRCh38 chr17: 2,448,182-2,448,182 , GRCh37.p13 chr17: 2,351,476-2,351,476 METTL16
    nsv5654709insertion1nstd207human GRCh38 chr17: 2,506,769-2,506,769 , GRCh37.p13 chr17: 2,410,063-2,410,063 METTL16
    nsv5597113copy number variation1nstd207human GRCh38 chr17: 2,491,652-2,491,987 , GRCh37.p13 chr17: 2,394,946-2,395,281 METTL16
    nsv5584639copy number variation1nstd207human GRCh38 chr17: 2,447,502-2,447,629 , GRCh37.p13 chr17: 2,350,796-2,350,923 METTL16
    nsv5559331inversion1nstd206human GRCh38 chr17: 2,497,010-2,497,700 , GRCh37.p13 chr17: 2,400,304-2,400,994 METTL16
    nsv5557616sequence alteration1nstd206human GRCh38 chr17: 2,497,050-2,498,096 , GRCh37.p13 chr17: 2,400,344-2,401,390 METTL16
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