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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv997076copy number variation1nstd45humanPathogenic GRCh37 chr7: 19,155,091-19,157,295 , GRCh38.p12 chr7: 19,115,468-19,117,672 TWIST1

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