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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv829272copy number variation4nstd67human NCBI36 chr22: 43,514,052-43,515,675 , GRCh37.p13 chr22: 45,135,388-45,137,011 , GRCh38.p12 chr22: 44,739,508-44,741,131 PRR5-ARHGAP8

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