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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    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
    nsv6863859copy number variation1nstd229human GRCh38 chr9: 21,398,074-21,398,294 , GRCh37.p13 chr9: 21,398,073-21,398,293 IFNA11P
    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
    nsv6434974copy number variation1nstd223human GRCh38 chr9: 21,398,301-21,406,900 , GRCh37.p13 chr9: 21,398,300-21,406,899 IFNA12P, IFNA11P
    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
    nsv6423172copy number variation1nstd223human GRCh38 chr9: 21,394,201-21,398,600 , GRCh37.p13 chr9: 21,394,200-21,398,599 IFNA11P
    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
    nsv6313892copy number variation1nstd102humanPathogenic GRCh37 chr9: 676,264-33,743,670 , GRCh38.p12 chr9: 676,264-33,743,672 SUGT1P1, FOCAD-AS1, 391 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
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