U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 944

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074833inversion1nstd229human GRCh38 chr9: 14,508,168-14,508,209 , GRCh37.p13 chr9: 14,508,166-14,508,207 NFIB
    nsv7072115inversion1nstd229human GRCh38 chr9: 12,276,809-15,153,662 , GRCh37.p13 chr9: 12,276,809-15,153,660 PES1P2, RNU6-559P, 30 more genes
    nsv7069060inversion1nstd229human GRCh38 chr9: 14,268,294-14,268,317 , GRCh37.p13 chr9: 14,268,293-14,268,316 NFIB
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7066663inversion1nstd229human GRCh38 chr9: 14,264,795-14,264,898 , GRCh37.p13 chr9: 14,264,794-14,264,897 NFIB
    nsv7065910inversion1nstd229human GRCh38 chr9: 13,576,634-14,660,296 , GRCh37.p13 chr9: 13,576,633-14,660,294 CDCA4P1, RPL3P11, 8 more genes
    nsv7063109inversion1nstd229human GRCh38 chr9: 14,407,583-14,409,528 , GRCh37.p13 chr9: 14,407,581-14,409,526 NFIB
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv6877895copy number variation1nstd229human GRCh38 chr9: 14,184,294-14,193,878 , GRCh37.p13 chr9: 14,184,293-14,193,877 NFIB
    nsv6877828copy number variation1nstd229human GRCh38 chr9: 14,204,110-14,209,053 , GRCh37.p13 chr9: 14,204,109-14,209,052 RPL7AP47, NFIB
    nsv6877648copy number variation1nstd229human GRCh38 chr9: 14,368,769-14,370,709 , GRCh37.p13 chr9: 14,368,768-14,370,708 NFIB
    nsv6877622copy number variation1nstd229human GRCh38 chr9: 14,226,508-15,063,519 , GRCh37.p13 chr9: 14,226,507-15,063,517 LDHAP4, CDCA4P1, 11 more genes
    nsv6877561copy number variation1nstd229human GRCh38 chr9: 14,246,809-14,249,903 , GRCh37.p13 chr9: 14,246,808-14,249,902 NFIB
    nsv6877430copy number variation1nstd229human GRCh38 chr9: 14,302,201-14,304,200 , GRCh37.p13 chr9: 14,302,200-14,304,199 NFIB
    nsv6876874copy number variation1nstd229human GRCh38 chr9: 14,520,501-14,525,200 , GRCh37.p13 chr9: 14,520,499-14,525,198 NFIB
    nsv6876042copy number variation1nstd229human GRCh38 chr9: 14,205,047-14,213,100 , GRCh37.p13 chr9: 14,205,046-14,213,099 RPL7AP47, NFIB
    nsv6875984copy number variation1nstd229human GRCh38 chr9: 12,949,792-14,402,752 , GRCh37.p13 chr9: 12,949,791-14,402,751 LINC00583, LOC101929507, 11 more genes
    nsv6875922copy number variation1nstd229human GRCh38 chr9: 14,201,401-14,205,300 , GRCh37.p13 chr9: 14,201,400-14,205,299 RPL7AP47, NFIB
    nsv6875012copy number variation1nstd229human GRCh38 chr9: 14,222,201-14,230,900 , GRCh37.p13 chr9: 14,222,200-14,230,899 NFIB
    nsv6873685copy number variation1nstd229human GRCh38 chr9: 14,452,786-14,453,390 , GRCh37.p13 chr9: 14,452,784-14,453,388 NFIB
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center