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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4423748copy number variation1nstd174human GRCh37 chr22: 45,134,832-45,138,958 , GRCh38.p12 chr22: 44,738,952-44,743,078 PRR5-ARHGAP8
    esv3647905copy number variation782estd214human GRCh37 chr22: 45,134,872-45,137,953 , GRCh38.p12 chr22: 44,738,992-44,742,073 PRR5-ARHGAP8

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