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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4641085mobile element deletion1nstd186human GRCh37 chr5: 156,084,730-156,093,914 , GRCh38.p12 chr5: 156,657,719-156,666,903 SGCD

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