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Items: 3

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    Number of Variants: 3

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4674237copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,942,610-227,945,265 , GRCh38.p12 chr2: 227,077,894-227,080,549 COL4A4
    nsv1397984copy number variation1nstd102humanPathogenic GRCh37 chr2: 227,958,838-227,958,889 , GRCh38 chr2: 227,094,122-227,094,173 COL4A4
    nsv4674766copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr2: 228,167,754-228,169,799 , GRCh38.p12 chr2: 227,303,038-227,305,083 MFF-DT, COL4A3
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