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Items: 1 to 20 of 327

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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
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv7059871inversion1nstd229human GRCh38 chr9: 21,046,765-21,059,694 , GRCh37.p13 chr9: 21,046,764-21,059,693 IFNNP1, LOC105375989
    nsv6873832copy number variation1nstd229human GRCh38 chr9: 20,684,201-21,311,600 , GRCh37.p13 chr9: 20,684,200-21,311,599 IFNWP5, IFNWP18, 22 more genes
    nsv6869797copy number variation1nstd229human GRCh38 chr9: 21,006,277-21,040,078 , GRCh37.p13 chr9: 21,006,276-21,040,077 HACD4, LOC105375989
    nsv6869544copy number variation1nstd229human GRCh38 chr9: 21,023,655-21,051,907 , GRCh37.p13 chr9: 21,023,654-21,051,906 LOC105375989, HACD4
    nsv6867634copy number variation1nstd229human GRCh38 chr9: 21,037,290-21,044,082 , GRCh37.p13 chr9: 21,037,289-21,044,081 LOC105375989
    nsv6866886copy number variation1nstd229human GRCh38 chr9: 20,629,960-21,204,461 , GRCh37.p13 chr9: 20,629,959-21,204,460 IFNA21, SNORA30B, 14 more genes
    nsv6864670copy number variation1nstd229human GRCh38 chr9: 21,038,118-21,284,709 , GRCh37.p13 chr9: 21,038,117-21,284,708 IFNWP18, IFNA17, 16 more genes
    nsv6864228copy number variation1nstd229human GRCh38 chr9: 20,929,721-21,121,933 , GRCh37.p13 chr9: 20,929,720-21,121,932 IFNB1, IFNWP4, 4 more genes
    nsv6862713copy number variation1nstd229human GRCh38 chr9: 20,907,116-21,046,221 , GRCh37.p13 chr9: 20,907,115-21,046,220 LOC105375989, HACD4, 1 more genes
    nsv6862412copy number variation1nstd229human GRCh38 chr9: 21,048,953-21,056,773 , GRCh37.p13 chr9: 21,048,952-21,056,772 IFNNP1, LOC105375989
    nsv6861701copy number variation1nstd229human GRCh38 chr9: 21,000,819-21,041,208 , GRCh37.p13 chr9: 21,000,818-21,041,207 HACD4, LOC105375989
    nsv6861041copy number variation1nstd229human GRCh38 chr9: 21,040,318-21,050,969 , GRCh37.p13 chr9: 21,040,317-21,050,968 LOC105375989
    nsv6860590copy number variation1nstd229human GRCh38 chr9: 21,041,301-21,045,000 , GRCh37.p13 chr9: 21,041,300-21,044,999 LOC105375989
    nsv6860296copy number variation1nstd229human GRCh38 chr9: 21,053,901-21,095,300 , GRCh37.p13 chr9: 21,053,900-21,095,299 IFNNP1, LOC105375989, 1 more genes
    nsv6859857copy number variation1nstd229human GRCh38 chr9: 21,051,889-21,180,148 , GRCh37.p13 chr9: 21,051,888-21,180,147 IFNWP4, LOC105375989, 5 more genes
    nsv6859216copy number variation1nstd229human GRCh38 chr9: 21,037,402-21,089,029 , GRCh37.p13 chr9: 21,037,401-21,089,028 IFNNP1, LOC105375989, 1 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
    nsv6637286copy number variation1nstd102humanUncertain significance GRCh37 chr9: 20,907,264-21,044,118 , GRCh38.p12 chr9: 20,907,265-21,044,119 LOC105375989, FOCAD, 1 more genes
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