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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6099insertion1nstd2human NCBI35 chr10: 24,926,597-24,956,736 , GRCh37.p13 chr10: 24,886,591-24,916,730 , GRCh38.p12 chr10: 24,597,662-24,627,801 ARHGAP21

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