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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4578342copy number variation1nstd182human GRCh38.p12 chr9: 136,481,478-136,540,904 , GRCh37 chr9: 139,375,930-139,435,356 NOTCH1, SEC16A, 2 more genes
    nsv4578341copy number variation1nstd182human GRCh38.p12 chr9: 136,357,558-136,540,904 , GRCh37 chr9: 139,252,010-139,435,356 NOTCH1, SNAPC4, 9 more genes

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