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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4458037tandem duplication1nstd102humanUncertain significance GRCh37 chr9: 135,803,187-135,807,265 , GRCh38.p12 chr9: 132,927,800-132,931,878 TSC1

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