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Items: 1 to 20 of 639

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5963056insertion1nstd209human GRCh38 chr3: 134,584,956-134,584,956 , GRCh37.p13 chr3: 134,303,798-134,303,798 CEP63
    nsv5960504insertion1nstd209human GRCh38 chr3: 134,547,614-134,547,614 , GRCh37.p13 chr3: 134,266,456-134,266,456 CEP63
    nsv5953858insertion1nstd209human GRCh38 chr3: 134,679,040-134,679,040 , GRCh37.p13 chr3: 134,397,882-134,397,882 EPHB1, CEP63
    nsv5901161copy number variation1nstd209human GRCh38 chr3: 134,615,529-134,615,699 , GRCh37.p13 chr3: 134,334,371-134,334,541 EPHB1, CEP63, 1 more genes
    nsv5898760copy number variation1nstd209human GRCh38 chr3: 134,756,494-134,757,745 , GRCh37.p13 chr3: 134,475,336-134,476,587 EPHB1, CEP63
    nsv5896286copy number variation1nstd209human GRCh38 chr3: 134,643,144-134,643,208 , GRCh37.p13 chr3: 134,361,986-134,362,050 EPHB1, CEP63, 1 more genes
    nsv5895335copy number variation1nstd209human GRCh38 chr3: 134,549,624-134,549,691 , GRCh37.p13 chr3: 134,268,466-134,268,533 CEP63
    nsv5892090copy number variation1nstd209human GRCh38 chr3: 134,539,517-134,543,867 , GRCh37.p13 chr3: 134,258,359-134,262,709 CEP63
    nsv5834916copy number variation1nstd209human GRCh38 chr3: 134,582,607-134,588,265 , GRCh37.p13 chr3: 134,301,449-134,307,107 CEP63
    nsv5834669copy number variation2nstd209human GRCh38 chr3: 134,756,714-134,757,913 , GRCh37.p13 chr3: 134,475,556-134,476,755 CEP63, EPHB1
    nsv5834667copy number variation1nstd209human GRCh38 chr3: 134,554,789-134,557,536 , GRCh37.p13 chr3: 134,273,631-134,276,378 CEP63
    nsv5834666copy number variation1nstd209human GRCh38 chr3: 134,539,660-134,543,942 , GRCh37.p13 chr3: 134,258,502-134,262,784 CEP63
    nsv5834321copy number variation2nstd209human GRCh38 chr3: 134,542,543-134,543,742 , GRCh37.p13 chr3: 134,261,385-134,262,584 CEP63
    nsv5694271mobile element insertion2nstd211human GRCh38 chr3: 134,679,053-134,679,053 , GRCh37.p13 chr3: 134,397,895-134,397,895 CEP63, EPHB1
    nsv5691677mobile element insertion1nstd211human GRCh38 chr3: 134,770,297-134,770,297 , GRCh37.p13 chr3: 134,489,139-134,489,139 EPHB1, CEP63
    nsv5685640mobile element insertion2nstd211human GRCh38 chr3: 134,727,987-134,727,987 , GRCh37.p13 chr3: 134,446,829-134,446,829 CEP63, EPHB1
    nsv5622292insertion1nstd207human GRCh38 chr3: 134,575,368-134,575,368 , GRCh37.p13 chr3: 134,294,210-134,294,210 CEP63
    nsv5614091insertion1nstd207human GRCh38 chr3: 134,701,277-134,701,277 , GRCh37.p13 chr3: 134,420,119-134,420,119 CEP63, EPHB1
    nsv5613139insertion1nstd207human GRCh38 chr3: 134,701,314-134,701,314 , GRCh37.p13 chr3: 134,420,156-134,420,156 CEP63, EPHB1
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