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Items: 1 to 20 of 453

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970591insertion1nstd209human GRCh38 chr13: 113,215,229-113,215,229 , GRCh37.p13 chr13: 113,869,543-113,869,543 , CUL4A
    nsv5967929insertion1nstd209human GRCh38 chr13: 113,260,203-113,260,203 , GRCh37.p13 chr13: 113,914,517-113,914,517 CUL4A
    nsv5937797copy number variation1nstd209human GRCh38 chr13: 113,211,902-113,211,955 , GRCh37.p13 chr13: 113,866,216-113,866,269 , CUL4A
    nsv5932957copy number variation1nstd209human GRCh38 chr13: 113,222,470-113,222,524 , GRCh37.p13 chr13: 113,876,784-113,876,838 CUL4A
    nsv5929359copy number variation1nstd209human GRCh38 chr13: 113,260,146-113,260,221 , GRCh37.p13 chr13: 113,914,460-113,914,535 CUL4A
    nsv5716381mobile element insertion2nstd211human GRCh38 chr13: 113,259,564-113,259,564 , GRCh37.p13 chr13: 113,913,878-113,913,878 CUL4A
    nsv5662753insertion2nstd207human GRCh38 chr13: 113,232,275-113,232,275 , GRCh37.p13 chr13: 113,886,589-113,886,589 CUL4A
    nsv5661534insertion1nstd207human GRCh38 chr13: 113,215,050-113,215,050 , GRCh37.p13 chr13: 113,869,364-113,869,364 , CUL4A
    nsv5656545insertion2nstd207human GRCh38 chr13: 113,263,139-113,263,139 , GRCh37.p13 chr13: 113,917,453-113,917,453 MIR8075, CUL4A
    nsv5654377insertion1nstd207human GRCh38 chr13: 113,232,154-113,232,154 , GRCh37.p13 chr13: 113,886,468-113,886,468 CUL4A
    nsv5651558insertion1nstd207human GRCh38 chr13: 113,262,779-113,262,779 , GRCh37.p13 chr13: 113,917,093-113,917,093 MIR8075, CUL4A
    nsv5649835insertion2nstd207human GRCh38 chr13: 113,232,039-113,232,039 , GRCh37.p13 chr13: 113,886,353-113,886,353 CUL4A
    nsv5648536insertion1nstd207human GRCh38 chr13: 113,232,197-113,232,197 , GRCh37.p13 chr13: 113,886,511-113,886,511 CUL4A
    nsv5646103insertion1nstd207human GRCh38 chr13: 113,232,250-113,232,250 , GRCh37.p13 chr13: 113,886,564-113,886,564 CUL4A
    nsv5598503copy number variation1nstd207human GRCh38 chr13: 113,232,097-113,232,189 , GRCh37.p13 chr13: 113,886,411-113,886,503 CUL4A
    nsv5587656copy number variation1nstd207human GRCh38 chr13: 113,215,750-113,215,836 , GRCh37.p13 chr13: 113,870,064-113,870,150 , CUL4A
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5538418insertion1nstd206human GRCh38 chr13: 113,211,696-113,211,736 , GRCh37.p13 chr13: 113,866,010-113,866,050 , CUL4A
    nsv5511518copy number variation1nstd206human GRCh38 chr13: 113,267,409-113,269,474 , GRCh37.p13 chr13: 113,921,723-113,923,788 CUL4A
    nsv5497376copy number variation1nstd206human GRCh38 chr13: 113,260,147-113,260,222 , GRCh37.p13 chr13: 113,914,461-113,914,536 CUL4A
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