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 82

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5661306insertion1nstd207human GRCh38 chr11: 17,050,533-17,050,533 , GRCh37.p13 chr11: 17,072,080-17,072,080 OR7E14P
    nsv5657661insertion1nstd207human GRCh38 chr11: 17,051,546-17,051,546 , GRCh37.p13 chr11: 17,073,093-17,073,093 OR7E14P
    nsv5653501insertion2nstd207human GRCh38 chr11: 17,050,441-17,050,441 , GRCh37.p13 chr11: 17,071,988-17,071,988 OR7E14P
    nsv5600758copy number variation1nstd207human GRCh38 chr11: 17,050,209-17,050,259 , GRCh37.p13 chr11: 17,071,756-17,071,806 OR7E14P
    nsv5598578copy number variation1nstd207human GRCh38 chr11: 17,050,275-17,050,531 , GRCh37.p13 chr11: 17,071,822-17,072,078 OR7E14P
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5032982mobile element deletion1nstd200human GRCh38 chr11: 17,049,579-17,051,677 , GRCh37.p13 chr11: 17,071,126-17,073,224 OR7E14P
    nsv4978406copy number variation1nstd200human GRCh38 chr11: 17,036,947-17,073,915 , GRCh37.p13 chr11: 17,058,494-17,095,462 SNORD14A, OR7E14P, 2 more genes
    nsv4873215mobile element deletion1nstd200human GRCh37 chr11: 17,071,125-17,073,225 , GRCh38.p12 chr11: 17,049,578-17,051,678 OR7E14P
    nsv4763736insertion1nstd199human GRCh37 chr11: 17,071,688-17,071,688 , GRCh38.p12 chr11: 17,050,141-17,050,141 OR7E14P
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4602717copy number variation1nstd183human GRCh37 chr11: 16,913,860-18,038,721 , GRCh38.p12 chr11: 16,892,313-18,017,174 , LINC02729, 27 more genes
    nsv4456716copy number variation1nstd102humanUncertain significance GRCh37 chr11: 16,775,884-18,418,719 , GRCh38.p12 chr11: 16,754,337-18,397,172 RNU6-593P, SNORD14A, 47 more genes
    nsv4456294copy number variation1nstd102humanUncertain significance GRCh37 chr11: 16,914,628-17,201,011 , GRCh38.p12 chr11: 16,893,081-17,179,464 RPL36AP37, PIK3C2A, 8 more genes
    nsv4455290copy number variation1nstd102humanUncertain significance GRCh37 chr11: 16,436,272-18,064,677 , GRCh38.p12 chr11: 16,414,726-18,043,130 LOC105376571, PIK3C2A, 30 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