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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7070239inversion1nstd229human GRCh38 chr9: 128,869,438-129,153,886 , GRCh37.p13 chr9: 131,631,717-131,916,165 DOLK, PTPA, 10 more genes
    nsv6877526copy number variation1nstd229human GRCh38 chr9: 129,142,552-129,147,384 , GRCh37.p13 chr9: 131,904,831-131,909,663 PTPA
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6308725mobile element insertion1nstd186human GRCh37 chr9: 131,905,507-131,905,558 , GRCh38.p12 chr9: 129,143,228-129,143,279 PTPA
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6142156copy number variation1nstd206human GRCh38 chr9: 129,036,552-129,154,552 , GRCh37.p13 chr9: 131,798,831-131,916,831 CRAT, DOLPP1, 2 more genes
    nsv6137057copy number variation1nstd213human GRCh37 chr9: 130,360,000-135,460,001 , GRCh38.p12 chr9: 127,597,721-132,584,614 CRAT, GLE1, 145 more genes
    nsv6018540copy number variation1nstd212human GRCh38 chr9: 129,123,335-129,123,423 , GRCh37.p13 chr9: 131,885,614-131,885,702 PTPA
    nsv5918584copy number variation1nstd209human GRCh38 chr9: 129,123,345-129,126,020 , GRCh37.p13 chr9: 131,885,624-131,888,299 PTPA
    nsv5863398copy number variation1nstd209human GRCh38 chr9: 129,127,063-129,129,465 , GRCh37.p13 chr9: 131,889,342-131,891,744 PTPA
    nsv5855092copy number variation1nstd209human GRCh38 chr9: 129,125,813-129,130,190 , GRCh37.p13 chr9: 131,888,092-131,892,469 PTPA
    nsv5848018copy number variation1nstd209human GRCh38 chr9: 129,123,563-129,125,962 , GRCh37.p13 chr9: 131,885,842-131,888,241 PTPA
    nsv5726508mobile element insertion2nstd211human GRCh38 chr9: 129,143,228-129,143,228 , GRCh37.p13 chr9: 131,905,507-131,905,507 PTPA
    nsv5634076insertion1nstd207human GRCh38 chr9: 129,127,307-129,127,307 , GRCh37.p13 chr9: 131,889,586-131,889,586 PTPA
    nsv5561928mobile element insertion1nstd206human GRCh38 chr9: 129,143,228-129,143,279 , GRCh37.p13 chr9: 131,905,507-131,905,558 PTPA
    nsv5492238copy number variation1nstd206human GRCh38 chr9: 129,130,415-129,132,588 , GRCh37.p13 chr9: 131,892,694-131,894,867 PTPA
    nsv5483650copy number variation1nstd206human GRCh38 chr9: 129,117,465-129,119,520 , GRCh37.p13 chr9: 131,879,744-131,881,799 PTPA
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