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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144156insertion1nstd232human GRCh37.p13 chr9: 35,102,830-35,102,830 , GRCh38.p12 chr9: 35,102,833-35,102,833 STOML2, ATOSB
    nsv7141294copy number variation1nstd232human GRCh37.p13 chr9: 35,101,807-35,101,898 , GRCh38.p12 chr9: 35,101,810-35,101,901 STOML2
    nsv7139202insertion1nstd232human GRCh37.p13 chr9: 35,101,279-35,101,279 , GRCh38.p12 chr9: 35,101,282-35,101,282 STOML2
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098082copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,370,797-36,276,941 , GRCh38.p12 chr9: 34,370,799-36,276,944 UNC13B, CD72, 86 more genes
    nsv7060440inversion1nstd229human GRCh38 chr9: 33,533,890-38,610,880 , GRCh37.p13 chr9: 33,533,888-38,610,877 FRMPD1, PTENP1, 182 more genes
    nsv7058978inversion1nstd229human GRCh38 chr9: 33,570,636-38,550,207 , GRCh37.p13 chr9: 33,570,634-38,550,204 TRBV29OR9-2, SPMIP6, 180 more genes
    nsv6870133copy number variation1nstd229human GRCh38 chr9: 34,043,094-35,876,103 , GRCh37.p13 chr9: 34,043,092-35,876,100 STOML2, ENHO, 85 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 more genes
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6142582copy number variation1nstd206human GRCh38 chr9: 35,098,000-35,106,000 , GRCh37.p13 chr9: 35,097,997-35,105,997 ATOSB, STOML2
    nsv6141848copy number variation1nstd206human GRCh38 chr9: 35,052,000-35,112,000 , GRCh37.p13 chr9: 35,051,997-35,111,997 PIGO, FANCG, 3 more genes
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
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