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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312788copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr7: 73,442,518-73,483,030 , GRCh38.p12 chr7: 74,028,188-74,068,700 0

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