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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1398044copy number variation1nstd102humanPathogenic NCBI36 chr21: 13,636,378-28,138,533 , GRCh37 chr21: 14,714,507-29,216,662 , GRCh38.p12 chr21: 13,342,186-27,844,343 LONRF2P5, RHOT1P2, 171 more genes

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