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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1071058copy number variation1nstd99human GRCh37 chr12: 118,498,499-118,499,200 , GRCh38.p12 chr12: 118,060,694-118,061,395 WSB2

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