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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv997154copy number variation1nstd45humanPathogenic GRCh37 chrX: 154,064,063-154,250,998 , GRCh38.p12 chrX: 154,835,788-155,022,723 F8, F8A1, 4 more genes
    nsv997128copy number variation1nstd45humanPathogenic GRCh37 chrX: 53,963,113-54,071,569 , GRCh38.p12 chrX: 53,936,680-54,045,136 PHF8

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