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 72

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070030inversion1nstd229human GRCh38 chr11: 16,966,270-21,356,221 , GRCh37.p13 chr11: 16,987,817-21,377,767 DBX1, PRMT3, 93 more genes
    nsv7067983inversion1nstd229human GRCh38 chr11: 17,304,327-18,032,820 , GRCh37.p13 chr11: 17,325,874-18,054,367 LOC107984317, LINC02729, 12 more genes
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6916591copy number variation1nstd229human GRCh38 chr11: 17,708,484-17,750,483 , GRCh37.p13 chr11: 17,730,031-17,772,030 MYOD1, KCNC1
    nsv6590311inversion1nstd223human GRCh38 chr11: 16,144,251-19,584,623 , GRCh37.p13 chr11: 16,165,797-19,606,170 LDHC, GLTPP1, 85 more genes
    nsv6441415copy number variation1nstd223human GRCh38 chr11: 17,708,484-17,750,480 , GRCh37.p13 chr11: 17,730,031-17,772,027 KCNC1, MYOD1
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6132090copy number variation1nstd213human GRCh37 chr11: 17,410,000-17,840,001 , GRCh38.p12 chr11: 17,388,453-17,818,454 KCNC1, KCNJ11, 7 more genes
    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
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 more genes
    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
    nsv4729618copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,461,542-17,773,192 , GRCh38.p12 chr11: 17,439,995-17,751,645 ABCC8, MYOD1, 4 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
    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