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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1160718copy number variation104nstd111human GRCh37 chr21: 44,968,053-44,973,667 , GRCh38.p12 chr21: 43,548,172-43,553,786 HSF2BP, RPL31P1

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