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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv829269copy number variation1nstd67human NCBI36 chr22: 43,513,960-43,515,463 , GRCh37.p13 chr22: 45,135,296-45,136,799 , GRCh38.p12 chr22: 44,739,416-44,740,919 PRR5-ARHGAP8

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