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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4425226copy number variation1nstd174human GRCh37 chr22: 29,679,408-29,681,896 , GRCh38.p12 chr22: 29,283,419-29,285,907 EWSR1
    esv3647529copy number variation129estd214human GRCh37 chr22: 29,679,404-29,681,913 , GRCh38.p12 chr22: 29,283,415-29,285,924 EWSR1

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