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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980373copy number variation2nstd102humanPathogenic GRCh37 chr11: 108,098,332-108,236,255 , GRCh38.p12 chr11: 108,227,605-108,365,528 C11orf65, ATM
    nsv4435814copy number variation1nstd102humanPathogenic GRCh38 chr17: 58,705,436-58,742,073 , GRCh37.p13 chr17: 56,782,797-56,819,434 LOC105371843, RAD51C

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