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 138

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5460174copy number variation1nstd206human GRCh38 chr6: 13,623,487-13,623,550 , GRCh37.p13 chr6: 13,623,719-13,623,782 RANBP9, NOL7
    nsv5378217translocation1nstd200human GRCh38 chr6: 13,629,768-13,629,768 , GRCh38 chr6: 13,630,804-13,630,804 , GRCh37.p13 chr6: 13,631,036-13,631,036 , GRCh37.p13 chr6: 13,630,000-13,630,000 NOL7, RANBP9
    nsv5378216translocation1nstd200human GRCh38 chr6: 13,623,550-13,623,550 , GRCh38 chr6: 13,623,487-13,623,487 , GRCh37.p13 chr6: 13,623,782-13,623,782 , GRCh37.p13 chr6: 13,623,719-13,623,719 RANBP9, NOL7
    nsv4809761copy number variation1nstd200human GRCh37 chr6: 13,630,000-13,631,036 , GRCh38.p12 chr6: 13,629,768-13,630,804 RANBP9, NOL7
    nsv4592013copy number variation1nstd183human GRCh37 chr6: 13,620,901-13,621,292 , GRCh38.p12 chr6: 13,620,669-13,621,060 NOL7, RANBP9
    nsv4540455insertion1nstd166human GRCh37.p13 chr6: 13,616,790-13,616,790 , GRCh38.p12 chr6: 13,616,558-13,616,558 NOL7
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4455888copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,248,587-18,083,552 , GRCh38.p12 chr6: 13,248,355-18,083,321 RNU6-522P, LOC105374942, 70 more genes
    nsv4395389copy number variation1nstd174human GRCh37 chr6: 13,622,143-13,710,600 , GRCh38.p12 chr6: 13,621,911-13,710,368 RANBP9, NOL7
    nsv4324882inversion1nstd166human GRCh37.p13 chr6: 11,087,007-14,472,606 , GRCh38.p12 chr6: 11,086,774-14,472,375 , HIVEP1, 56 more genes
    nsv4128196copy number variation1nstd166human GRCh37.p13 chr6: 13,623,719-13,623,782 , GRCh38.p12 chr6: 13,623,487-13,623,550 NOL7, RANBP9
    nsv4112646copy number variation1nstd166human GRCh37.p13 chr6: 13,630,000-13,631,036 , GRCh38.p12 chr6: 13,629,768-13,630,804 RANBP9, NOL7
    nsv3924426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,232,627-13,805,381 , GRCh38 chr6: 13,232,395-13,805,149 , NCBI36 chr6: 13,340,606-13,913,360 LOC105374936, RN7SKP204, 12 more genes
    nsv3922594copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,311,751-16,295,791 , GRCh38 chr6: 13,311,519-16,295,560 , NCBI36 chr6: 13,419,730-16,403,770 LOC107986571, LOC105374947, 47 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3918220copy number variation1nstd102humanPathogenic GRCh38 chr6: 10,601,499-13,987,316 , NCBI36 chr6: 10,709,718-14,095,526 , GRCh37 chr6: 10,601,732-13,987,547 GCNT2, LOC105374935, 58 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3913657copy number variation1nstd102humanPathogenic NCBI36 chr6: 51,431-18,468,805 , GRCh38 chr6: 106,431-18,360,595 , GRCh37 chr6: 106,431-18,360,826 LOC105374904, CAP2, 294 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