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 95

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054647inversion1nstd229human GRCh38 chr6: 125,609,155-134,343,808 , GRCh37.p13 chr6: 125,930,301-134,664,946 RPS12, TMEM244, 130 more genes
    nsv7053719inversion1nstd229human GRCh38 chr6: 125,606,974-134,343,957 , GRCh37.p13 chr6: 125,928,120-134,665,095 SNORD100, SLC18B1, 130 more genes
    nsv7040961inversion1nstd229human GRCh38 chr6: 131,090,546-134,695,837 , GRCh37.p13 chr6: 131,411,686-135,016,975 ENPP3, MOXD1, 70 more genes
    nsv7038109inversion1nstd229human GRCh38 chr6: 125,606,921-134,343,957 , GRCh37.p13 chr6: 125,928,067-134,665,095 PTPRK-AS1, MED23, 130 more genes
    nsv6813456copy number variation1nstd229human GRCh38 chr6: 132,514,345-132,599,634 , GRCh37.p13 chr6: 132,835,484-132,920,773 TAAR8, TAAR6, 5 more genes
    nsv6811868copy number variation1nstd229human GRCh38 chr6: 132,478,988-132,558,798 , GRCh37.p13 chr6: 132,800,127-132,879,937 RPL21P66, TAAR8, 3 more genes
    nsv6800626copy number variation1nstd229human GRCh38 chr6: 132,533,002-132,673,328 , GRCh37.p13 chr6: 132,854,141-132,994,467 TAAR7P, TAAR6, 8 more genes
    nsv6630666copy number variation1nstd224human GRCh37 chr6: 132,835,222-132,920,150 , GRCh38.p12 chr6: 132,514,083-132,599,011 TAAR5, TAAR8, 5 more genes
    nsv6563707inversion1nstd223human GRCh38 chr6: 125,606,968-134,343,906 , GRCh37.p13 chr6: 125,928,114-134,665,044 TAAR2, LOC105377996, 130 more genes
    nsv6315321copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791 SLC18B1, ARHGAP18, 223 more genes
    nsv6290946copy number variation1nstd102humanPathogenic GRCh37 chr6: 130,769,034-136,009,217 , GRCh38.p12 chr6: 130,447,889-135,688,079 LOC105378004, LINC01010, 89 more genes
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945686copy number variation1nstd200human GRCh38 chr6: 132,526,677-132,551,822 , GRCh37.p13 chr6: 132,847,816-132,872,961 TAAR8, TAAR9
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv3962697copy number variation1nstd168human GRCh38 chr6: 132,501,376-132,543,100 , GRCh37.p13 chr6: 132,822,515-132,864,239 STX7, TAAR9, 1 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 KATNA1, RNF217-AS1, 422 more genes
    nsv3914780copy number variation1nstd102humanUncertain significance NCBI36 chr6: 132,860,706-132,969,136 , GRCh37.p13 chr6: 132,819,013-132,927,443 , GRCh38.p12 chr6: 132,497,874-132,606,304 TAAR8, TAAR6, 7 more genes
    nsv3913689copy number variation1nstd102humanPathogenic NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272 TPD52L1, MESTP1, 316 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