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 136

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5887344copy number variation1nstd209human GRCh38 chr16: 66,940,257-66,948,699 , GRCh37.p13 chr16: 66,974,160-66,982,602 LOC107984881, CES2
    nsv5709050mobile element insertion1nstd211human GRCh38 chr16: 66,944,324-66,944,324 , GRCh37.p13 chr16: 66,978,227-66,978,227 CES2
    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
    nsv5271075copy number variation1nstd204human GRCh38.p13 chr16: 66,941,232-66,949,831 , GRCh37.p13 chr16: 66,975,135-66,983,734 LOC107984881, CES2
    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
    nsv5005776copy number variation1nstd200human GRCh38 chr16: 66,935,725-66,948,986 , GRCh37.p13 chr16: 66,969,628-66,982,889 LOC107984881, CES2
    nsv4993079copy number variation1nstd200human GRCh38 chr16: 66,936,022-66,948,988 , GRCh37.p13 chr16: 66,969,925-66,982,891 CES2, LOC107984881
    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
    nsv4864201copy number variation1nstd200human GRCh37 chr16: 66,969,628-66,982,889 , GRCh38.p12 chr16: 66,935,725-66,948,986 CES2, LOC107984881
    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
    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
    nsv4243712copy number variation1nstd166human GRCh37.p13 chr16: 66,970,000-66,983,000 , GRCh38.p12 chr16: 66,936,097-66,949,097 LOC107984881, CES2
    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