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Items: 11

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    Number of Variants: 11

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3912778copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,498,433-55,348,528 , GRCh38 chr3: 49,461,000-55,314,500 , NCBI36 chr3: 49,473,437-55,323,568 CISH, SEMA3G, 160 more genes
    nsv4728146copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,807,193-51,363,558 , GRCh38.p12 chr3: 48,769,760-51,326,127 CISH, APEH, 90 more genes
    nsv6311990copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,547,968-50,685,477 , GRCh38.p12 chr3: 49,510,535-50,648,046 CISH, APEH, 52 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 CISH, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 CISH, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 CISH, RPL23AP49, 2875 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 CISH, UQCRC1, 291 more genes
    nsv3921797copy number variation1nstd102humanPathogenic NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353 CISH, RBM5-AS1, 185 more genes
    nsv6311797copy number variation1nstd102humanUncertain significance GRCh37 chr3: 50,431,520-50,685,477 , GRCh38.p12 chr3: 50,394,089-50,648,046 CISH, CACNA2D2, 6 more genes
    nsv6311798copy number variation1nstd102humanUncertain significance GRCh37 chr3: 50,540,629-50,655,235 , GRCh38.p12 chr3: 50,503,198-50,617,804 CISH, MAPKAPK3, 4 more genes
    nsv3883874copy number variation1nstd102humanUncertain significance GRCh37 chr3: 50,435,928-50,732,729 , GRCh38.p12 chr3: 50,398,497-50,695,298 CISH, MIR4787, 10 more genes
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