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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3842807mobile element deletion197estd219human GRCh37 chr5: 156,084,721-156,093,924 , GRCh38.p12 chr5: 156,657,710-156,666,913 SGCD

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