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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv6877427copy number variation1nstd229human GRCh38 chr9: 21,326,735-21,430,048 , GRCh37.p13 chr9: 21,326,734-21,430,047 IFNA8, IFNA11P, 7 more genes
    nsv6877388copy number variation1nstd229human GRCh38 chr9: 21,310,217-22,111,393 , GRCh37.p13 chr9: 21,310,216-22,111,392 UBA52P6, KHSRPP1, 23 more genes
    nsv6874838copy number variation1nstd229human GRCh38 chr9: 21,336,282-21,368,008 , GRCh37.p13 chr9: 21,336,281-21,368,007 IFNA13, LOC107987053, 1 more genes
    nsv6869556copy number variation1nstd229human GRCh38 chr9: 21,133,080-21,557,410 , GRCh37.p13 chr9: 21,133,079-21,557,409 IFNWP19, IFNWP2, 27 more genes
    nsv6864846copy number variation1nstd229human GRCh38 chr9: 21,348,014-21,369,921 , GRCh37.p13 chr9: 21,348,013-21,369,920 IFNA6, IFNA13
    nsv6864494copy number variation1nstd229human GRCh38 chr9: 21,355,071-21,408,400 , GRCh37.p13 chr9: 21,355,070-21,408,399 IFNA8, IFNA2, 3 more genes
    nsv6860759copy number variation1nstd229human GRCh38 chr9: 21,368,201-21,368,700 , GRCh37.p13 chr9: 21,368,200-21,368,699 IFNA13
    nsv6858882copy number variation1nstd229human GRCh38 chr9: 21,365,598-21,390,671 , GRCh37.p13 chr9: 21,365,597-21,390,670 IFNA13, IFNA2
    nsv6858537copy number variation1nstd229human GRCh38 chr9: 21,276,100-21,574,776 , GRCh37.p13 chr9: 21,276,099-21,574,775 IFNA2, IFNA20P, 15 more genes
    nsv6637750copy number variation1nstd102humanUncertain significance GRCh37 chr9: 20,659,492-22,347,440 , GRCh38.p12 chr9: 20,659,493-22,347,441 CDKN2B, IFNA10, 46 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
    nsv6633251copy number variation1nstd224human GRCh37 chr9: 20,976,421-21,415,687 , GRCh38.p12 chr9: 20,976,422-21,415,688 IFNA5, IFNA16, 27 more genes
    nsv6562498inversion1nstd223human GRCh38 chr9: 20,655,689-27,693,631 , GRCh37.p13 chr9: 20,655,688-27,693,629 IFNA7, IFNW1, 92 more genes
    nsv6424642copy number variation1nstd223human GRCh38 chr9: 21,276,100-21,574,774 , GRCh37.p13 chr9: 21,276,099-21,574,773 IFNA11P, IFNE, 15 more genes
    nsv6423408copy number variation1nstd223human GRCh38 chr9: 21,365,598-21,390,670 , GRCh37.p13 chr9: 21,365,597-21,390,669 IFNA13, IFNA2
    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
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