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Items: 1 to 20 of 2372

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117844copy number variation1nstd186human GRCh37 chr3: 131,677,806-131,678,143 , GRCh38.p12 chr3: 131,958,962-131,959,299 CPNE4
    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
    nsv5969248inversion1nstd209human GRCh38 chr3: 131,969,007-131,978,042 , GRCh37.p13 chr3: 131,687,851-131,696,886 CPNE4
    nsv5968616inversion1nstd209human GRCh38 chr3: 131,989,407-131,989,567 , GRCh37.p13 chr3: 131,708,251-131,708,411 CPNE4
    nsv5967415insertion1nstd209human GRCh38 chr3: 132,148,101-132,148,101 , GRCh37.p13 chr3: 131,866,945-131,866,945 CPNE4
    nsv5966995insertion1nstd209human GRCh38 chr3: 132,256,856-132,256,856 , GRCh37.p13 chr3: 131,975,700-131,975,700 CPNE4
    nsv5965351insertion1nstd209human GRCh38 chr3: 131,952,457-131,952,457 , GRCh37.p13 chr3: 131,671,301-131,671,301 CPNE4
    nsv5964462insertion1nstd209human GRCh38 chr3: 131,792,623-131,792,623 , GRCh37.p13 chr3: 131,511,467-131,511,467 CPNE4
    nsv5956617insertion1nstd209human GRCh38 chr3: 132,005,343-132,005,343 , GRCh37.p13 chr3: 131,724,187-131,724,187 CPNE4
    nsv5950684insertion1nstd209human GRCh38 chr3: 132,235,252-132,235,252 , GRCh37.p13 chr3: 131,954,096-131,954,096 CPNE4
    nsv5950164insertion1nstd209human GRCh38 chr3: 132,172,924-132,172,924 , GRCh37.p13 chr3: 131,891,768-131,891,768 CPNE4
    nsv5907148copy number variation1nstd209human GRCh38 chr3: 131,827,305-131,828,123 , GRCh37.p13 chr3: 131,546,149-131,546,967 LOC105374113, CPNE4
    nsv5907086copy number variation1nstd209human GRCh38 chr3: 132,144,453-132,144,767 , GRCh37.p13 chr3: 131,863,297-131,863,611 CPNE4
    nsv5906987copy number variation1nstd209human GRCh38 chr3: 131,814,562-131,814,902 , GRCh37.p13 chr3: 131,533,406-131,533,746 CPNE4, LOC105374113
    nsv5906864copy number variation1nstd209human GRCh38 chr3: 131,607,573-131,607,675 , GRCh37.p13 chr3: 131,326,417-131,326,519 CPNE4
    nsv5906520copy number variation1nstd209human GRCh38 chr3: 131,954,135-131,963,888 , GRCh37.p13 chr3: 131,672,979-131,682,732 CPNE4
    nsv5906247copy number variation1nstd209human GRCh38 chr3: 131,958,958-131,959,298 , GRCh37.p13 chr3: 131,677,802-131,678,142 CPNE4
    nsv5905953copy number variation1nstd209human GRCh38 chr3: 131,635,818-131,636,092 , GRCh37.p13 chr3: 131,354,662-131,354,936 CPNE4
    nsv5904815copy number variation1nstd209human GRCh38 chr3: 132,229,099-132,231,796 , GRCh37.p13 chr3: 131,947,943-131,950,640 CPNE4, TRC-GCA6-1, 1 more genes
    nsv5904461copy number variation1nstd209human GRCh38 chr3: 131,752,402-131,752,904 , GRCh37.p13 chr3: 131,471,246-131,471,748 CPNE4
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