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 138

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924676copy number variation1nstd209human GRCh38 chr12: 9,058,448-9,058,505 , GRCh37.p13 chr12: 9,211,044-9,211,101 LINC00612, KLRG1
    nsv5660044insertion1nstd207human GRCh38 chr12: 9,062,065-9,062,065 , GRCh37.p13 chr12: 9,214,661-9,214,661 KLRG1, LINC00612
    nsv5651952insertion1nstd207human GRCh38 chr12: 9,062,355-9,062,355 , GRCh37.p13 chr12: 9,214,951-9,214,951 KLRG1, LINC00612
    nsv5588443copy number variation1nstd207human GRCh38 chr12: 9,062,355-9,062,411 , GRCh37.p13 chr12: 9,214,951-9,215,007 KLRG1, LINC00612
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5216514mobile element deletion1nstd204human GRCh37.p13 chr12: 9,212,566-9,212,945 , GRCh38.p13 chr12: 9,059,970-9,060,349 KLRG1, LINC00612
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4972142copy number variation1nstd200human GRCh38 chr12: 9,058,327-9,059,373 , GRCh37.p13 chr12: 9,210,923-9,211,969 KLRG1, LINC00612
    nsv4899747mobile element deletion1nstd200human GRCh38 chr12: 9,059,972-9,060,363 , GRCh37.p13 chr12: 9,212,568-9,212,959 LINC00612, KLRG1
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4775034mobile element deletion1nstd200human GRCh37 chr12: 9,212,568-9,212,959 , GRCh38.p12 chr12: 9,059,972-9,060,363 KLRG1, LINC00612
    nsv4749480copy number variation1nstd199human GRCh38.p12 chr12: 9,065,149-9,065,241 , GRCh37 chr12: 9,217,745-9,217,837 KLRG1, A2M-AS1, 1 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4616824copy number variation1nstd183human GRCh37 chr12: 8,488,721-9,625,223 , GRCh38.p12 chr12: 8,336,125-9,472,627 , BTG1P1, 43 more genes
    nsv4605464copy number variation1nstd183human GRCh37 chr12: 9,217,785-9,217,847 , GRCh38.p12 chr12: 9,065,189-9,065,251 A2M-AS1, KLRG1, 1 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4455054copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,966,269-9,289,695 , GRCh38.p12 chr12: 8,813,673-9,137,099 M6PR, A2M, 8 more genes
    nsv4372959copy number variation1nstd173human GRCh37 chr12: 9,158,245-9,218,636 , GRCh38.p12 chr12: 9,005,649-9,066,040 A2M, KLRG1, 3 more genes
    nsv4350818copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,216-15,001,420 , GRCh38.p12 chr12: 80,050-14,848,486 LOC107984495, KLRC1, 432 more genes
    nsv4324171inversion1nstd166human GRCh37.p13 chr12: 6,338,819-22,046,498 , GRCh38.p12 chr12: 6,229,653-21,893,564 , APOBEC1, 414 more genes
    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