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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5976967insertion1nstd209human GRCh38 chr16: 56,624,558-56,624,558 , GRCh37.p13 chr16: 56,658,470-56,658,470 MT1E
    nsv5929985copy number variation1nstd209human GRCh38 chr16: 56,619,255-56,661,122 , GRCh37.p13 chr16: 56,653,167-56,695,034 MT1DP, MT1A, 8 more genes
    nsv5885009copy number variation1nstd209human GRCh38 chr16: 56,619,240-56,660,960 , GRCh37.p13 chr16: 56,653,152-56,694,872 LOC101927536, MT1E, 8 more genes
    nsv5695888mobile element insertion2nstd211human GRCh38 chr16: 56,627,048-56,627,048 , GRCh37.p13 chr16: 56,660,960-56,660,960 MT1E
    nsv5525141copy number variation1nstd206human GRCh38 chr16: 56,626,482-56,683,244 , GRCh37.p13 chr16: 56,660,394-56,717,156 MT1B, MT1H, 11 more genes
    nsv5424635mobile element insertion1nstd206human GRCh38 chr16: 56,627,048-56,627,099 , GRCh37.p13 chr16: 56,660,960-56,661,011 MT1E
    nsv5314506copy number variation1nstd204human GRCh38.p13 chr16: 56,626,187-56,683,500 , GRCh37.p13 chr16: 56,660,099-56,717,412 MT1F, MT1CP, 11 more genes
    nsv5280014copy number variation1nstd204human GRCh37.p13 chr16: 56,660,174-56,696,547 , GRCh38.p13 chr16: 56,626,262-56,662,635 MT1A, MT1B, 7 more genes
    nsv5274913copy number variation1nstd204human GRCh38.p13 chr16: 56,626,501-56,683,200 , GRCh37.p13 chr16: 56,660,413-56,717,112 MT1X, MT1JP, 11 more genes
    nsv5274017copy number variation1nstd204human GRCh38.p13 chr16: 56,627,439-56,628,438 , GRCh37.p13 chr16: 56,661,351-56,662,350 MT1E
    nsv5152344mobile element insertion1nstd203human GRCh38 chr16: 56,627,031-56,627,048 , GRCh37.p13 chr16: 56,660,943-56,660,960 MT1E
    nsv5008362copy number variation1nstd200human GRCh38 chr16: 56,626,606-56,633,498 , GRCh37.p13 chr16: 56,660,518-56,667,410 MT1M, MT1E
    nsv5005697copy number variation1nstd200human GRCh38 chr16: 56,621,050-56,630,260 , GRCh37.p13 chr16: 56,654,962-56,664,172 MT1E
    nsv5005696copy number variation1nstd200human GRCh38 chr16: 56,618,007-56,626,449 , GRCh37.p13 chr16: 56,651,919-56,660,361 MT1L, MT1E
    nsv4864166copy number variation1nstd200human GRCh37 chr16: 56,660,334-56,717,181 , GRCh38.p12 chr16: 56,626,422-56,683,269 MT1X, LOC101927536, 11 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4622165copy number variation1nstd183human GRCh37 chr16: 56,653,019-56,714,520 , GRCh38.p12 chr16: 56,619,107-56,680,608 MT1L, MT1CP, 12 more genes
    nsv4503573mobile element insertion1nstd166human GRCh37.p13 chr16: 56,660,943-56,660,943 , GRCh38.p12 chr16: 56,627,031-56,627,031 MT1E
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
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