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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877607copy number variation1nstd102humanPathogenic GRCh37 chr11: 83,315,294-86,755,595 , GRCh38.p12 chr11: 83,604,251-87,044,553 OR7E13P, PICALM, 43 more genes
    nsv997194copy number variation1nstd45humanPathogenic GRCh37 chr11: 86,656,717-86,666,440 , GRCh38.p12 chr11: 86,945,675-86,955,398 FZD4, PRSS23, 1 more genes

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