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Items: 1 to 20 of 693

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131421insertion1nstd186human GRCh37 chr14: 73,820,292-73,820,292 , GRCh38.p12 chr14: 73,353,584-73,353,584 NUMB
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5978831inversion1nstd209human GRCh38 chr14: 73,368,321-73,368,506 , GRCh37.p13 chr14: 73,835,029-73,835,214 NUMB
    nsv5977126insertion1nstd209human GRCh38 chr14: 73,440,246-73,440,246 , GRCh37.p13 chr14: 73,906,954-73,906,954 NUMB
    nsv5972342insertion1nstd209human GRCh38 chr14: 73,353,584-73,353,584 , GRCh37.p13 chr14: 73,820,292-73,820,292 NUMB
    nsv5970073insertion1nstd209human GRCh38 chr14: 73,332,740-73,332,740 , GRCh37.p13 chr14: 73,799,448-73,799,448 NUMB
    nsv5946862copy number variation1nstd209human GRCh38 chr14: 73,369,137-73,369,474 , GRCh37.p13 chr14: 73,835,845-73,836,182 NUMB
    nsv5933211copy number variation1nstd209human GRCh38 chr14: 73,281,372-73,281,859 , GRCh37.p13 chr14: 73,748,080-73,748,567 NUMB
    nsv5928254copy number variation1nstd209human GRCh38 chr14: 73,382,228-73,386,961 , GRCh37.p13 chr14: 73,848,936-73,853,669 NUMB
    nsv5856719copy number variation1nstd209human GRCh38 chr14: 73,382,170-73,386,649 , GRCh37.p13 chr14: 73,848,878-73,853,357 NUMB
    nsv5722625mobile element insertion2nstd211human GRCh38 chr14: 73,328,452-73,328,452 , GRCh37.p13 chr14: 73,795,160-73,795,160 NUMB
    nsv5710660mobile element insertion1nstd211human GRCh38 chr14: 73,328,452-73,328,452 , GRCh37.p13 chr14: 73,795,160-73,795,160 NUMB
    nsv5707302mobile element insertion1nstd211human GRCh38 chr14: 73,391,893-73,391,893 , GRCh37.p13 chr14: 73,858,601-73,858,601 NUMB
    nsv5705209mobile element insertion1nstd211human GRCh38 chr14: 73,352,501-73,352,501 , GRCh37.p13 chr14: 73,819,209-73,819,209 NUMB
    nsv5701852mobile element insertion2nstd211human GRCh38 chr14: 73,358,144-73,358,144 , GRCh37.p13 chr14: 73,824,852-73,824,852 NUMB
    nsv5653092insertion1nstd207human GRCh38 chr14: 73,332,739-73,332,739 , GRCh37.p13 chr14: 73,799,447-73,799,447 NUMB
    nsv5651497insertion1nstd207human GRCh38 chr14: 73,353,584-73,353,584 , GRCh37.p13 chr14: 73,820,292-73,820,292 NUMB
    nsv5649641insertion1nstd207human GRCh38 chr14: 73,294,866-73,294,866 , GRCh37.p13 chr14: 73,761,574-73,761,574 NUMB
    nsv5600778copy number variation1nstd207human GRCh38 chr14: 73,352,455-73,352,514 , GRCh37.p13 chr14: 73,819,163-73,819,222 NUMB
    nsv5559302mobile element insertion1nstd206human GRCh38 chr14: 73,328,452-73,328,503 , GRCh37.p13 chr14: 73,795,160-73,795,211 NUMB
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