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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315105copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,783,902-133,788,747 , GRCh38 chr6: 133,462,764-133,467,609 EYA4
    nsv997028copy number variation1nstd45humanPathogenic GRCh38.p12 chr6: 133,241,357-133,532,120 , GRCh37 chr6: 133,562,495-133,853,258 EYA4, TARID, 1 more genes

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