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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1026359copy number variation2nstd100human NCBI36 chr7: 276,088-326,216 , GRCh37.p13 chr7: 181,005-231,133 , GRCh38.p12 chr7: 181,005-231,133 FAM20C, LOC105375116

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