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Items: 1 to 20 of 346

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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
    nsv5971910insertion1nstd209human GRCh38 chr16: 50,182,891-50,182,891 , GRCh37.p13 chr16: 50,216,802-50,216,802 TENT4B
    nsv5946939copy number variation1nstd209human GRCh38 chr16: 50,221,621-50,222,874 , GRCh37.p13 chr16: 50,255,532-50,256,785 TENT4B
    nsv5944802copy number variation1nstd209human GRCh38 chr16: 50,158,045-50,158,366 , GRCh37.p13 chr16: 50,191,956-50,192,277 TENT4B
    nsv5942544copy number variation1nstd209human GRCh38 chr16: 50,189,606-50,191,163 , GRCh37.p13 chr16: 50,223,517-50,225,074 TENT4B
    nsv5940458copy number variation1nstd209human GRCh38 chr16: 50,187,418-50,192,076 , GRCh37.p13 chr16: 50,221,329-50,225,987 TENT4B
    nsv5928659copy number variation1nstd209human GRCh38 chr16: 50,168,956-50,173,987 , GRCh37.p13 chr16: 50,202,867-50,207,898 TENT4B
    nsv5884826copy number variation2nstd209human GRCh38 chr16: 50,190,183-50,191,382 , GRCh37.p13 chr16: 50,224,094-50,225,293 TENT4B
    nsv5877770copy number variation1nstd209human GRCh38 chr16: 50,169,150-50,174,075 , GRCh37.p13 chr16: 50,203,061-50,207,986 TENT4B
    nsv5869221copy number variation1nstd209human GRCh38 chr16: 50,187,383-50,191,382 , GRCh37.p13 chr16: 50,221,294-50,225,293 TENT4B
    nsv5713736mobile element insertion1nstd211human GRCh38 chr16: 50,169,413-50,169,413 , GRCh37.p13 chr16: 50,203,324-50,203,324 TENT4B
    nsv5713450mobile element insertion1nstd211human GRCh38 chr16: 50,182,922-50,182,922 , GRCh37.p13 chr16: 50,216,833-50,216,833 TENT4B
    nsv5706823mobile element insertion1nstd211human GRCh38 chr16: 50,211,704-50,211,704 , GRCh37.p13 chr16: 50,245,615-50,245,615 TENT4B
    nsv5552778insertion1nstd206human GRCh38 chr16: 50,164,175-50,164,182 , GRCh37.p13 chr16: 50,198,086-50,198,093 TENT4B
    nsv5533403copy number variation1nstd206human GRCh38 chr16: 50,173,960-50,176,773 , GRCh37.p13 chr16: 50,207,871-50,210,684 TENT4B
    nsv5529602copy number variation1nstd206human GRCh38 chr16: 50,187,393-50,192,108 , GRCh37.p13 chr16: 50,221,304-50,226,019 TENT4B
    nsv5525050copy number variation1nstd206human GRCh38 chr16: 50,189,608-50,191,164 , GRCh37.p13 chr16: 50,223,519-50,225,075 TENT4B
    nsv5515375copy number variation1nstd206human GRCh38 chr16: 50,227,547-50,227,601 , GRCh37.p13 chr16: 50,261,458-50,261,512 TENT4B
    nsv5430917mobile element insertion1nstd206human GRCh38 chr16: 50,211,704-50,211,755 , GRCh37.p13 chr16: 50,245,615-50,245,666 TENT4B
    nsv5309700copy number variation1nstd204human GRCh38.p13 chr16: 50,187,159-50,192,370 , GRCh37.p13 chr16: 50,221,070-50,226,281 TENT4B
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