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Items: 1 to 20 of 546

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971637insertion1nstd209human GRCh38 chr12: 38,710,268-38,710,268 , GRCh37.p13 chr12: 39,104,070-39,104,070 CPNE8
    nsv5969393insertion1nstd209human GRCh38 chr12: 38,749,343-38,749,343 , GRCh37.p13 chr12: 39,143,145-39,143,145 CPNE8
    nsv5967770insertion1nstd209human GRCh38 chr12: 38,854,386-38,854,386 , GRCh37.p13 chr12: 39,248,188-39,248,188 CPNE8
    nsv5942865copy number variation1nstd209human GRCh38 chr12: 38,656,618-38,660,885 , GRCh37.p13 chr12: 39,050,420-39,054,687 CPNE8
    nsv5939803copy number variation1nstd209human GRCh38 chr12: 38,793,163-38,793,267 , GRCh37.p13 chr12: 39,186,965-39,187,069 CPNE8
    nsv5939320copy number variation1nstd209human GRCh38 chr12: 38,803,730-38,806,860 , GRCh37.p13 chr12: 39,197,532-39,200,662 CPNE8
    nsv5938044copy number variation1nstd209human GRCh38 chr12: 38,661,480-38,661,645 , GRCh37.p13 chr12: 39,055,282-39,055,447 CPNE8
    nsv5929467copy number variation1nstd209human GRCh38 chr12: 38,697,449-38,697,498 , GRCh37.p13 chr12: 39,091,251-39,091,300 CPNE8
    nsv5867517copy number variation1nstd209human GRCh38 chr12: 38,773,548-38,775,593 , GRCh37.p13 chr12: 39,167,350-39,169,395 CPNE8
    nsv5858642copy number variation1nstd209human GRCh38 chr12: 38,656,607-38,660,990 , GRCh37.p13 chr12: 39,050,409-39,054,792 CPNE8
    nsv5857415copy number variation1nstd209human GRCh38 chr12: 38,741,898-38,745,591 , GRCh37.p13 chr12: 39,135,700-39,139,393 CPNE8
    nsv5857376copy number variation1nstd209human GRCh38 chr12: 38,796,952-38,800,126 , GRCh37.p13 chr12: 39,190,754-39,193,928 CPNE8
    nsv5857361copy number variation1nstd209human GRCh38 chr12: 38,658,257-38,662,035 , GRCh37.p13 chr12: 39,052,059-39,055,837 CPNE8
    nsv5849789copy number variation1nstd209human GRCh38 chr12: 38,770,548-38,772,797 , GRCh37.p13 chr12: 39,164,350-39,166,599 CPNE8
    nsv5715423mobile element insertion2nstd211human GRCh38 chr12: 38,690,102-38,690,102 , GRCh37.p13 chr12: 39,083,904-39,083,904 CPNE8
    nsv5708901mobile element insertion2nstd211human GRCh38 chr12: 38,727,773-38,727,773 , GRCh37.p13 chr12: 39,121,575-39,121,575 CPNE8
    nsv5644730insertion1nstd207human GRCh38 chr12: 38,854,386-38,854,386 , GRCh37.p13 chr12: 39,248,188-39,248,188 CPNE8
    nsv5599927copy number variation1nstd207human GRCh38 chr12: 38,803,763-38,806,856 , GRCh37.p13 chr12: 39,197,565-39,200,658 CPNE8
    nsv5596722copy number variation1nstd207human GRCh38 chr12: 38,793,163-38,793,267 , GRCh37.p13 chr12: 39,186,965-39,187,069 CPNE8
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
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