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 413

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7073731inversion1nstd229human GRCh38 chr11: 66,869,382-66,869,510 , GRCh37.p13 chr11: 66,636,853-66,636,981 PC
    nsv6917730copy number variation1nstd229human GRCh38 chr11: 66,873,623-66,883,045 , GRCh37.p13 chr11: 66,641,094-66,650,516 PC
    nsv6912757copy number variation1nstd229human GRCh38 chr11: 66,793,001-68,121,500 , GRCh37.p13 chr11: 66,560,472-67,888,967 CHKA-DT, LOC107984341, 66 more genes
    nsv6911594copy number variation1nstd229human GRCh38 chr11: 66,890,517-66,891,433 , GRCh37.p13 chr11: 66,657,988-66,658,904 PC
    nsv6908803copy number variation1nstd229human GRCh38 chr11: 66,735,625-66,857,769 , GRCh37.p13 chr11: 66,503,096-66,625,240 PC, FTLP6, 4 more genes
    nsv6908779copy number variation1nstd229human GRCh38 chr11: 66,930,360-66,936,816 , GRCh37.p13 chr11: 66,697,831-66,704,287 PC, MIR3163
    nsv6908355copy number variation1nstd229human GRCh38 chr11: 66,920,497-66,950,682 , GRCh37.p13 chr11: 66,687,968-66,718,153 PC, MIR3163
    nsv6908086copy number variation1nstd229human GRCh38 chr11: 66,897,319-66,904,387 , GRCh37.p13 chr11: 66,664,790-66,671,858 PC
    nsv6908011copy number variation1nstd229human GRCh38 chr11: 66,902,028-66,919,982 , GRCh37.p13 chr11: 66,669,499-66,687,453 RNU7-23P, PC
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6904660copy number variation1nstd229human GRCh38 chr11: 66,859,080-66,950,102 , GRCh37.p13 chr11: 66,626,551-66,717,573 MIR3163, PC, 2 more genes
    nsv6904167copy number variation1nstd229human GRCh38 chr11: 66,930,720-66,941,055 , GRCh37.p13 chr11: 66,698,191-66,708,526 PC, MIR3163
    nsv6902312copy number variation1nstd229human GRCh38 chr11: 66,920,956-66,928,306 , GRCh37.p13 chr11: 66,688,427-66,695,777 PC
    nsv6900064copy number variation1nstd229human GRCh38 chr11: 66,934,863-66,938,240 , GRCh37.p13 chr11: 66,702,334-66,705,711 MIR3163, PC
    nsv6900037copy number variation1nstd229human GRCh38 chr11: 66,932,599-66,935,949 , GRCh37.p13 chr11: 66,700,070-66,703,420 PC, MIR3163
    nsv6590465inversion1nstd223human GRCh38 chr11: 66,940,217-66,940,704 , GRCh37.p13 chr11: 66,707,688-66,708,175 PC
    nsv6584719inversion1nstd223human GRCh38 chr11: 66,941,592-66,942,965 , GRCh37.p13 chr11: 66,709,063-66,710,436 PC
    nsv6581712inversion1nstd223human GRCh38 chr11: 66,923,310-66,923,586 , GRCh37.p13 chr11: 66,690,781-66,691,057 PC
    nsv6474816copy number variation1nstd223human GRCh38 chr11: 66,883,312-66,883,559 , GRCh37.p13 chr11: 66,650,783-66,651,030 PC
    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