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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3582933copy number variation15estd212human GRCh37 chr18: 673,646-677,339 , GRCh38.p12 chr18: 673,646-677,339 TYMS, ENOSF1

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