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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315173copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,766,313-74,042,787 , GRCh38.p12 chr7: 73,352,304-74,628,471 0

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