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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096095copy number variation1nstd102humanPathogenic GRCh37 chr21: 38,269,150-38,269,441 , GRCh38.p12 chr21: 36,896,850-36,897,141 HLCS
    nsv7095920copy number variation1nstd102humanLikely pathogenic GRCh37 chr21: 38,126,547-38,139,606 , GRCh38.p12 chr21: 36,754,246-36,767,305 HLCS
    nsv7073521inversion1nstd229human GRCh38 chr21: 36,750,767-37,285,523 , GRCh37.p13 chr21: 38,123,068-38,657,825 HLCS, DPRXP5, 11 more genes
    nsv7070448inversion1nstd229human GRCh38 chr21: 36,987,449-36,989,511 , GRCh37.p13 chr21: 38,359,749-38,361,811 HLCS
    nsv7070054inversion1nstd229human GRCh38 chr21: 36,940,155-36,982,744 , GRCh37.p13 chr21: 38,312,455-38,355,044 DPRXP5, HLCS
    nsv7064129inversion1nstd229human GRCh38 chr21: 36,976,107-36,986,332 , GRCh37.p13 chr21: 38,348,407-38,358,632 HLCS
    nsv7060386inversion1nstd229human GRCh38 chr21: 34,646,865-38,528,329 , GRCh37.p13 chr21: 36,019,164-39,900,253 , TTC3-AS1, 70 more genes
    nsv7037393copy number variation1nstd229human GRCh38 chr21: 36,771,274-36,771,642 , GRCh37.p13 chr21: 38,143,575-38,143,943 HLCS
    nsv7037133copy number variation1nstd229human GRCh38 chr21: 36,937,537-36,942,063 , GRCh37.p13 chr21: 38,309,837-38,314,363 HLCS, DPRXP5
    nsv7036091copy number variation1nstd229human GRCh38 chr21: 36,790,401-36,884,300 , GRCh37.p13 chr21: 38,162,702-38,256,600 RNA5SP491, HLCS, 1 more genes
    nsv7035694copy number variation1nstd229human GRCh38 chr21: 36,778,972-36,785,481 , GRCh37.p13 chr21: 38,151,273-38,157,782 HLCS
    nsv7035367copy number variation1nstd229human GRCh38 chr21: 36,983,273-36,989,179 , GRCh37.p13 chr21: 38,355,573-38,361,479 HLCS
    nsv7035070copy number variation1nstd229human GRCh38 chr21: 36,973,748-36,987,352 , GRCh37.p13 chr21: 38,346,048-38,359,652 HLCS
    nsv7034374copy number variation1nstd229human GRCh38 chr21: 36,810,379-36,813,118 , GRCh37.p13 chr21: 38,182,680-38,185,418 LOC105369305, HLCS
    nsv7033309copy number variation1nstd229human GRCh38 chr21: 36,914,656-36,914,839 , GRCh37.p13 chr21: 38,286,956-38,287,139 HLCS
    nsv7033174copy number variation1nstd229human GRCh38 chr21: 36,981,843-37,000,835 , GRCh37.p13 chr21: 38,354,143-38,373,135 HLCS, MRPL20P1
    nsv7032309copy number variation1nstd229human GRCh38 chr21: 36,785,453-37,053,700 , GRCh37.p13 chr21: 38,157,754-38,426,000 RNA5SP491, RIPPLY3, 5 more genes
    nsv7030365copy number variation1nstd229human GRCh38 chr21: 36,793,242-36,812,641 , GRCh37.p13 chr21: 38,165,543-38,184,941 LOC105369305, HLCS
    nsv7029816copy number variation1nstd229human GRCh38 chr21: 36,858,821-36,904,187 , GRCh37.p13 chr21: 38,231,121-38,276,487 HLCS
    nsv7029406copy number variation1nstd229human GRCh38 chr21: 36,846,129-36,853,230 , GRCh37.p13 chr21: 38,218,429-38,225,530 HLCS, RNA5SP491
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