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Items: 1 to 20 of 1037

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967654inversion1nstd209human GRCh38 chr5: 33,778,534-33,778,590 , GRCh37.p13 chr5: 33,778,639-33,778,695 ADAMTS12
    nsv5953699insertion1nstd209human GRCh38 chr5: 33,596,176-33,596,176 , GRCh37.p13 chr5: 33,596,281-33,596,281 ADAMTS12
    nsv5952651insertion1nstd209human GRCh38 chr5: 33,797,438-33,797,438 , GRCh37.p13 chr5: 33,797,543-33,797,543 ADAMTS12
    nsv5905786copy number variation1nstd209human GRCh38 chr5: 33,688,357-33,688,423 , GRCh37.p13 chr5: 33,688,462-33,688,528 ADAMTS12
    nsv5902165copy number variation1nstd209human GRCh37.p13 chr5: 33,280,515-33,574,694 , GRCh38 chr5: 33,280,409-33,574,589 TARS1, ADAMTS12, 4 more genes
    nsv5900380copy number variation1nstd209human GRCh38 chr5: 33,726,616-33,726,956 , GRCh37.p13 chr5: 33,726,721-33,727,061 ADAMTS12
    nsv5898730copy number variation1nstd209human GRCh38 chr5: 33,626,770-33,627,023 , GRCh37.p13 chr5: 33,626,875-33,627,128 ADAMTS12
    nsv5897746copy number variation1nstd209human GRCh38 chr5: 33,550,276-33,553,172 , GRCh37.p13 chr5: 33,550,381-33,553,277 ADAMTS12
    nsv5894981copy number variation1nstd209human GRCh38 chr5: 33,843,410-33,846,176 , GRCh37.p13 chr5: 33,843,515-33,846,281 ADAMTS12
    nsv5893184copy number variation1nstd209human GRCh38 chr5: 33,280,300-33,574,357 , GRCh37.p13 chr5: 33,280,406-33,574,462 TARS1, ADAMTS12, 4 more genes
    nsv5890916copy number variation1nstd209human GRCh38 chr5: 33,626,416-33,626,478 , GRCh37.p13 chr5: 33,626,521-33,626,583 ADAMTS12
    nsv5889380copy number variation1nstd209human GRCh38 chr5: 33,626,344-33,626,621 , GRCh37.p13 chr5: 33,626,449-33,626,726 ADAMTS12
    nsv5842962copy number variation1nstd209human GRCh38 chr5: 33,842,844-33,845,872 , GRCh37.p13 chr5: 33,842,949-33,845,977 ADAMTS12
    nsv5842397copy number variation1nstd209human GRCh38 chr5: 33,550,380-33,553,079 , GRCh37.p13 chr5: 33,550,485-33,553,184 ADAMTS12
    nsv5729496mobile element insertion2nstd211human GRCh38 chr5: 33,797,452-33,797,452 , GRCh37.p13 chr5: 33,797,557-33,797,557 ADAMTS12
    nsv5729387mobile element insertion1nstd211human GRCh38 chr5: 33,837,086-33,837,086 , GRCh37.p13 chr5: 33,837,191-33,837,191 ADAMTS12
    nsv5720972mobile element insertion2nstd211human GRCh38 chr5: 33,633,243-33,633,243 , GRCh37.p13 chr5: 33,633,348-33,633,348 ADAMTS12
    nsv5720556mobile element insertion1nstd211human GRCh38 chr5: 33,837,123-33,837,123 , GRCh37.p13 chr5: 33,837,228-33,837,228 ADAMTS12
    nsv5716355mobile element insertion2nstd211human GRCh38 chr5: 33,551,833-33,551,833 , GRCh37.p13 chr5: 33,551,938-33,551,938 ADAMTS12
    nsv5714515mobile element insertion1nstd211human GRCh38 chr5: 33,575,265-33,575,265 , GRCh37.p13 chr5: 33,575,370-33,575,370 ADAMTS12
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