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Items: 4

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    Number of Variants: 4

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315194delins1nstd102humanPathogenic GRCh37 chr22: 31,012,077-31,014,228 , GRCh38 chr22: 30,616,090-30,618,241 TCN2
    nsv6311183copy number variation1nstd102humanPathogenic GRCh37 chr22: 31,003,319-31,022,508 , GRCh38.p12 chr22: 30,607,332-30,626,521 TCN2, PES1
    nsv5564413copy number variation1nstd102humanUncertain significance GRCh37 chr22: 31,008,840-31,013,502 , GRCh38.p12 chr22: 30,612,853-30,617,515 TCN2
    nsv4450734copy number variation1nstd102humanPathogenic GRCh38 chr22: 30,612,853-30,615,807 , GRCh37 chr22: 31,008,840-31,011,794 TCN2
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