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Items: 1 to 20 of 633

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072719inversion1nstd229human GRCh38 chr9: 14,792,079-19,156,478 , GRCh37.p13 chr9: 14,792,077-19,156,476 RN7SL98P, RRAGA, 49 more genes
    nsv7071645inversion1nstd229human GRCh38 chr9: 15,300,530-15,302,975 , GRCh37.p13 chr9: 15,300,528-15,302,973 TTC39B
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv6877994copy number variation1nstd229human GRCh38 chr9: 15,186,736-15,188,579 , GRCh37.p13 chr9: 15,186,734-15,188,577 TTC39B
    nsv6877501copy number variation1nstd229human GRCh38 chr9: 15,238,918-15,252,581 , GRCh37.p13 chr9: 15,238,916-15,252,579 TTC39B
    nsv6876812copy number variation1nstd229human GRCh38 chr9: 15,260,672-15,274,378 , GRCh37.p13 chr9: 15,260,670-15,274,376 TTC39B
    nsv6876793copy number variation1nstd229human GRCh38 chr9: 15,304,947-15,305,014 , GRCh37.p13 chr9: 15,304,945-15,305,012 TTC39B
    nsv6876365copy number variation1nstd229human GRCh38 chr9: 15,190,501-15,261,700 , GRCh37.p13 chr9: 15,190,499-15,261,698 TTC39B
    nsv6875817copy number variation1nstd229human GRCh38 chr9: 15,286,418-15,290,717 , GRCh37.p13 chr9: 15,286,416-15,290,715 TTC39B
    nsv6875386copy number variation1nstd229human GRCh38 chr9: 15,228,550-15,241,824 , GRCh37.p13 chr9: 15,228,548-15,241,822 TTC39B
    nsv6875209copy number variation1nstd229human GRCh38 chr9: 15,152,901-15,163,500 , GRCh37.p13 chr9: 15,152,899-15,163,498 TTC39B
    nsv6874949copy number variation1nstd229human GRCh38 chr9: 15,279,171-15,307,584 , GRCh37.p13 chr9: 15,279,169-15,307,582 TTC39B
    nsv6874435copy number variation1nstd229human GRCh38 chr9: 15,189,397-15,189,526 , GRCh37.p13 chr9: 15,189,395-15,189,524 TTC39B
    nsv6872112copy number variation1nstd229human GRCh38 chr9: 15,272,974-15,329,768 , GRCh37.p13 chr9: 15,272,972-15,329,766 TTC39B
    nsv6870562copy number variation1nstd229human GRCh38 chr9: 15,192,751-15,194,364 , GRCh37.p13 chr9: 15,192,749-15,194,362 TTC39B
    nsv6870352copy number variation1nstd229human GRCh38 chr9: 15,288,201-15,372,700 , GRCh37.p13 chr9: 15,288,199-15,372,698 RPL7P33, TTC39B
    nsv6869498copy number variation1nstd229human GRCh38 chr9: 15,223,801-15,234,200 , GRCh37.p13 chr9: 15,223,799-15,234,198 TTC39B
    nsv6869278copy number variation1nstd229human GRCh38 chr9: 15,143,001-15,162,300 , GRCh37.p13 chr9: 15,142,999-15,162,298 TTC39B, RNU6-559P
    nsv6868976copy number variation1nstd229human GRCh38 chr9: 15,246,386-15,506,731 , GRCh37.p13 chr9: 15,246,384-15,506,729 SNAPC3, RNU6-319P, 3 more genes
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