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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2671408copy number variation86estd199human GRCh37 chr2: 138,735,145-138,737,792 , GRCh38.p12 chr2: 137,977,575-137,980,222 HNMT, LOC107985948

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