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Items: 1 to 20 of 859

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074914inversion1nstd229human GRCh38 chr9: 17,621,837-17,661,233 , GRCh37.p13 chr9: 17,621,835-17,661,231 SH3GL2
    nsv7074707inversion1nstd229human GRCh38 chr9: 17,635,055-17,685,784 , GRCh37.p13 chr9: 17,635,053-17,685,782 SH3GL2
    nsv7072719inversion1nstd229human GRCh38 chr9: 14,792,079-19,156,478 , GRCh37.p13 chr9: 14,792,077-19,156,476 RN7SL98P, RRAGA, 49 more genes
    nsv7070595inversion1nstd229human GRCh38 chr9: 17,581,636-17,631,036 , GRCh37.p13 chr9: 17,581,634-17,631,034 PABPC1P11, SH3GL2
    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
    nsv6877528copy number variation1nstd229human GRCh38 chr9: 17,625,780-17,641,289 , GRCh37.p13 chr9: 17,625,778-17,641,287 SH3GL2
    nsv6876449copy number variation1nstd229human GRCh38 chr9: 17,628,425-17,628,454 , GRCh37.p13 chr9: 17,628,423-17,628,452 SH3GL2
    nsv6876295copy number variation1nstd229human GRCh38 chr9: 17,680,997-17,722,918 , GRCh37.p13 chr9: 17,680,995-17,722,916 SH3GL2
    nsv6874549copy number variation1nstd229human GRCh38 chr9: 17,581,688-17,634,314 , GRCh37.p13 chr9: 17,581,686-17,634,312 PABPC1P11, SH3GL2
    nsv6873994copy number variation1nstd229human GRCh38 chr9: 17,684,288-17,690,453 , GRCh37.p13 chr9: 17,684,286-17,690,451 SH3GL2
    nsv6872013copy number variation1nstd229human GRCh38 chr9: 17,624,699-17,674,648 , GRCh37.p13 chr9: 17,624,697-17,674,646 SH3GL2
    nsv6871844copy number variation1nstd229human GRCh38 chr9: 17,701,675-17,706,232 , GRCh37.p13 chr9: 17,701,673-17,706,230 SH3GL2
    nsv6871514copy number variation1nstd229human GRCh38 chr9: 17,598,401-17,840,548 , GRCh37.p13 chr9: 17,598,399-17,840,546 SH3GL2
    nsv6870594copy number variation1nstd229human GRCh38 chr9: 17,580,846-17,580,988 , GRCh37.p13 chr9: 17,580,844-17,580,986 SH3GL2
    nsv6870558copy number variation1nstd229human GRCh38 chr9: 17,606,598-17,616,507 , GRCh37.p13 chr9: 17,606,596-17,616,505 SH3GL2
    nsv6869368copy number variation1nstd229human GRCh38 chr9: 17,745,101-17,747,100 , GRCh37.p13 chr9: 17,745,099-17,747,098 SH3GL2
    nsv6868760copy number variation1nstd229human GRCh38 chr9: 17,761,515-17,761,585 , GRCh37.p13 chr9: 17,761,513-17,761,583 SH3GL2
    nsv6867768copy number variation1nstd229human GRCh38 chr9: 17,165,352-20,022,245 , GRCh37.p13 chr9: 17,165,350-20,022,243 SH3GL2, SLC24A2, 31 more genes
    nsv6867673copy number variation1nstd229human GRCh38 chr9: 17,710,328-17,763,843 , GRCh37.p13 chr9: 17,710,326-17,763,841 SH3GL2
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