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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv9918copy number variation8nstd4human NCBI35 chr22: 43,455,369-43,459,493 , GRCh37.p13 chr22: 45,134,832-45,138,956 , GRCh38.p12 chr22: 44,738,952-44,743,076 PRR5-ARHGAP8

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