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 153

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5910946copy number variation1nstd209human GRCh38 chr12: 8,608,228-8,608,278 , GRCh37.p13 chr12: 8,760,824-8,760,874 AICDA
    nsv5644546insertion1nstd207human GRCh38 chr12: 8,608,228-8,608,228 , GRCh37.p13 chr12: 8,760,824-8,760,824 AICDA
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4974316copy number variation1nstd200human GRCh38 chr12: 8,482,988-8,890,234 , GRCh37.p13 chr12: 8,635,584-9,042,830 MFAP5, SUPT4H1P2, 10 more genes
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4765994insertion1nstd199human GRCh37 chr12: 8,760,861-8,760,861 , GRCh38.p12 chr12: 8,608,265-8,608,265 AICDA
    nsv4681960copy number variation1nstd102humanPathogenic GRCh37 chr12: 8,608,708-8,765,363 , GRCh38.p12 chr12: 8,456,112-8,612,767 CLEC4E, AICDA, 6 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
    nsv4616796copy number variation1nstd183human GRCh37 chr12: 8,529,392-8,773,126 , GRCh38.p12 chr12: 8,376,796-8,620,530 OR7E148P, LOC105369645, 10 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
    nsv4455042copy number variation4nstd102humanUncertain significance GRCh37 chr12: 6,945,914-9,027,627 , GRCh38.p12 chr12: 6,836,750-8,875,031 HADHAP2, CLEC6A, 91 more genes
    nsv4454652copy number variation1nstd102humanPathogenic GRCh37 chr12: 8,756,860-8,765,383 , GRCh38 chr12: 8,604,264-8,612,787 AICDA
    nsv4387082copy number variation1nstd173human GRCh37 chr12: 8,716,307-9,033,700 , GRCh38.p12 chr12: 8,563,711-8,881,104 AICDA, HADHAP2, 6 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
    nsv4199177copy number variation1nstd166human GRCh37.p13 chr12: 8,527,733-8,779,242 , GRCh38.p12 chr12: 8,375,137-8,626,646 RNU6-275P, AICDA, 10 more genes
    nsv3971839copy number variation1nstd102humannot provided GRCh38 chr12: 1-9,000,000 , GRCh37.p13 chr12: 282,465-9,152,596 RNU4ATAC16P, RNU6-174P, 257 more genes
    nsv3924262copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104 ENO2, SLC6A13, 684 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