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 146

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935871copy number variation1nstd209human GRCh38 chr16: 66,968,419-66,970,358 , GRCh37.p13 chr16: 67,002,322-67,004,261 CES3
    nsv5927890copy number variation1nstd209human GRCh38 chr16: 66,940,488-67,029,326 , GRCh37.p13 chr16: 66,974,391-67,063,229 CBFB, CES2, 4 more genes
    nsv5883990copy number variation1nstd209human GRCh38 chr16: 66,962,013-66,964,712 , GRCh37.p13 chr16: 66,995,916-66,998,615 CES3
    nsv5882913copy number variation2nstd209human GRCh38 chr16: 66,968,581-66,969,825 , GRCh37.p13 chr16: 67,002,484-67,003,728 CES3
    nsv5532815copy number variation1nstd206human GRCh38 chr16: 66,940,488-67,029,328 , GRCh37.p13 chr16: 66,974,391-67,063,231 CBFB, CES2, 4 more genes
    nsv5518218copy number variation1nstd206human GRCh38 chr16: 66,964,312-66,964,754 , GRCh37.p13 chr16: 66,998,215-66,998,657 CES3
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005777copy number variation1nstd200human GRCh38 chr16: 66,940,488-67,029,328 , GRCh37.p13 chr16: 66,974,391-67,063,231 CES3, LOC107984881, 4 more genes
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4864202copy number variation1nstd200human GRCh37 chr16: 66,974,391-67,063,231 , GRCh38.p12 chr16: 66,940,488-67,029,328 CES3, CES4A, 4 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4675201copy number variation1nstd102humanPathogenic GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280 LOC100420066, LINC00920, 143 more genes
    nsv4500328mobile element insertion1nstd166human GRCh37.p13 chr16: 67,007,031-67,007,031 , GRCh38.p12 chr16: 66,973,128-66,973,128 CES3
    nsv4456092copy number variation1nstd102humanUncertain significance GRCh37 chr16: 66,797,153-67,109,495 , GRCh38.p12 chr16: 66,763,250-67,075,592 CES4A, RN7SL543P, 12 more genes
    nsv4455939copy number variation1nstd102humanUncertain significance GRCh37 chr16: 66,876,199-67,150,370 , GRCh38.p12 chr16: 66,842,296-67,116,467 CDH16, CA7, 11 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4332560sequence alteration1nstd166human GRCh37.p13 chr16: 57,901,049-75,540,778 , GRCh38.p12 chr16: 57,867,145-75,506,880 , AGRP, 331 more genes
    nsv4244968copy number variation1nstd166human GRCh37.p13 chr16: 66,998,078-66,998,657 , GRCh38.p12 chr16: 66,964,175-66,964,754 CES3
    nsv4236316copy number variation1nstd166human GRCh37.p13 chr16: 66,997,830-66,998,612 , GRCh38.p12 chr16: 66,963,927-66,964,709 CES3
    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