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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944357copy number variation1nstd209human GRCh38 chr14: 28,960,481-28,960,693 , GRCh37.p13 chr14: 29,429,687-29,429,899 LINC02327
    nsv5939833copy number variation1nstd209human GRCh38 chr14: 28,865,515-28,865,588 , GRCh37.p13 chr14: 29,334,721-29,334,794 LINC02327
    nsv5939218copy number variation1nstd209human GRCh38 chr14: 28,964,245-28,964,297 , GRCh37.p13 chr14: 29,433,451-29,433,503 LINC02327
    nsv5719030mobile element insertion1nstd211human GRCh38 chr14: 28,962,196-28,962,196 , GRCh37.p13 chr14: 29,431,402-29,431,402 LINC02327
    nsv5709223mobile element insertion2nstd211human GRCh38 chr14: 28,884,325-28,884,325 , GRCh37.p13 chr14: 29,353,531-29,353,531 LINC02327
    nsv5696448mobile element insertion2nstd211human GRCh38 chr14: 28,917,188-28,917,188 , GRCh37.p13 chr14: 29,386,394-29,386,394 LINC02327
    nsv5511887copy number variation1nstd206human GRCh38 chr14: 28,960,481-28,960,714 , GRCh37.p13 chr14: 29,429,687-29,429,920 LINC02327
    nsv5498952copy number variation1nstd206human GRCh38 chr14: 28,865,515-28,865,593 , GRCh37.p13 chr14: 29,334,721-29,334,799 LINC02327
    nsv5494775copy number variation1nstd206human GRCh38 chr14: 28,894,303-28,894,496 , GRCh37.p13 chr14: 29,363,509-29,363,702 LINC02327
    nsv5425662mobile element insertion1nstd206human GRCh38 chr14: 28,917,188-28,917,239 , GRCh37.p13 chr14: 29,386,394-29,386,445 LINC02327
    nsv5423142mobile element insertion1nstd206human GRCh38 chr14: 28,884,325-28,884,376 , GRCh37.p13 chr14: 29,353,531-29,353,582 LINC02327
    nsv5381770copy number variation1nstd102humanPathogenic GRCh37 chr14: 27,450,705-31,529,481 , GRCh38.p12 chr14: 26,981,499-31,060,275 RPS27AP4, LINC00645, 43 more genes
    nsv5374472translocation1nstd200human GRCh38 chr20: 16,149,208-16,149,208 , GRCh38 chr14: 28,900,991-28,900,991 , GRCh37.p13 chr14: 29,370,197-29,370,197 , GRCh37.p13 chr20: 16,129,853-16,129,853 LINC02327
    nsv5349080translocation1nstd200human GRCh38 chr14: 28,960,481-28,960,481 , GRCh38 chr14: 28,960,698-28,960,698 , GRCh37.p13 chr14: 29,429,904-29,429,904 , GRCh37.p13 chr14: 29,429,687-29,429,687 LINC02327
    nsv5349079translocation1nstd200human GRCh38 chr14: 28,865,593-28,865,593 , GRCh38 chr14: 28,865,515-28,865,515 , GRCh37.p13 chr14: 29,334,721-29,334,721 , GRCh37.p13 chr14: 29,334,799-29,334,799 LINC02327
    nsv5330966translocation1nstd200human GRCh37 chr14: 29,429,904-29,429,904 , GRCh37 chr14: 29,429,687-29,429,687 , GRCh38.p12 chr14: 28,960,481-28,960,481 , GRCh38.p12 chr14: 28,960,698-28,960,698 LINC02327
    nsv5309166copy number variation1nstd204human GRCh38.p13 chr14: 28,847,865-28,849,260 , GRCh37.p13 chr14: 29,317,071-29,318,466 LINC02327
    nsv5301930copy number variation1nstd204human GRCh38.p13 chr14: 28,960,458-28,960,722 , GRCh37.p13 chr14: 29,429,664-29,429,928 LINC02327
    nsv5206589mobile element deletion1nstd204human GRCh38.p13 chr14: 28,873,873-28,874,186 , GRCh37.p13 chr14: 29,343,079-29,343,392 LINC02327
    nsv5196678mobile element insertion1nstd203human GRCh38 chr14: 28,925,329-28,925,346 , GRCh37.p13 chr14: 29,394,535-29,394,552 LINC02327
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