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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314985copy number variation1nstd102humanUncertain risk allele GRCh37 chr15: 2,897-2,953 , GRCh38.p12 chr: NaN-NaN 0

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