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Items: 1 to 20 of 183

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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
    nsv6869641copy number variation1nstd229human GRCh38 chr9: 129,831,525-129,941,719 , GRCh37.p13 chr9: 132,593,804-132,703,998 MIR6855, USP20, 2 more genes
    nsv6866387copy number variation1nstd229human GRCh38 chr9: 129,698,067-130,033,998 , GRCh37.p13 chr9: 132,460,346-132,796,277 USP20, FNBP1, 8 more genes
    nsv6865389copy number variation1nstd229human GRCh38 chr9: 129,827,301-129,831,900 , GRCh37.p13 chr9: 132,589,580-132,594,179 C9orf78
    nsv6861356copy number variation1nstd229human GRCh38 chr9: 129,677,229-130,203,315 , GRCh37.p13 chr9: 132,439,508-132,892,849 USP20, UBE2V1P4, 11 more genes
    nsv6637875copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,449,937-132,807,448 , GRCh38.p12 chr9: 129,687,658-130,045,169 PRRX2-AS1, USP20, 8 more genes
    nsv6633149copy number variation1nstd224human GRCh37 chr9: 132,541,344-132,978,477 , GRCh38.p12 chr9: 129,779,065-130,216,198 USP20, NCS1, 8 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6301935copy number variation1nstd186human GRCh37 chr9: 132,595,117-132,595,416 , GRCh38.p12 chr9: 129,832,838-129,833,137 C9orf78
    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
    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
    nsv5492209copy number variation1nstd206human GRCh38 chr9: 129,832,838-129,833,137 , GRCh37.p13 chr9: 132,595,117-132,595,416 C9orf78
    nsv5483905copy number variation1nstd206human GRCh38 chr9: 129,698,067-130,033,998 , GRCh37.p13 chr9: 132,460,346-132,796,277 MIR6855, PRRX2, 8 more genes
    nsv5250774copy number variation1nstd204human GRCh38.p13 chr9: 129,443,501-129,853,600 , GRCh37.p13 chr9: 132,205,780-132,615,879 ASB6, C9orf50, 12 more genes
    nsv5246717copy number variation1nstd204human GRCh37.p13 chr9: 132,524,680-132,876,179 , GRCh38.p13 chr9: 129,762,401-130,113,900 TOR1A, USP20, 6 more genes
    nsv5189783mobile element insertion1nstd203human GRCh38 chr9: 129,826,478-129,826,486 , GRCh37.p13 chr9: 132,588,757-132,588,765 C9orf78
    nsv4988475copy number variation1nstd200human GRCh38 chr9: 129,828,066-129,834,935 , GRCh37.p13 chr9: 132,590,345-132,597,214 C9orf78, USP20
    nsv4729432copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,470,092-133,044,256 , GRCh38.p12 chr9: 129,707,813-130,281,977 GPRACR, NCS1, 13 more genes
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