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 123

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899267copy number variation1nstd209human GRCh38 chr6: 42,957,850-43,031,425 , GRCh37.p13 chr6: 42,925,588-42,999,163 MEA1, PEX6, 5 more genes
    nsv5887689copy number variation1nstd209human GRCh38 chr6: 43,026,845-43,026,904 , GRCh37.p13 chr6: 42,994,583-42,994,642 RRP36
    nsv5845514copy number variation1nstd209human GRCh38 chr6: 43,006,921-43,029,742 , GRCh37.p13 chr6: 42,974,659-42,997,480 MEA1, PPP2R5D, 2 more genes
    nsv5844905copy number variation2nstd209human GRCh38 chr6: 43,023,587-43,025,186 , GRCh37.p13 chr6: 42,991,325-42,992,924 RRP36
    nsv5844904copy number variation1nstd209human GRCh38 chr6: 43,022,756-43,023,786 , GRCh37.p13 chr6: 42,990,494-42,991,524 RRP36
    nsv5673766copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749 SRF, POLR1C, 39 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5332488translocation1nstd200human GRCh37 chr6: 42,989,496-42,989,496 , GRCh37 chr6: 42,989,428-42,989,428 , GRCh38.p12 chr6: 43,021,758-43,021,758 , GRCh38.p12 chr6: 43,021,690-43,021,690 RRP36, KLHDC3
    nsv5224950copy number variation1nstd204human GRCh38.p13 chr6: 42,543,301-43,041,600 , GRCh37.p13 chr6: 42,511,039-43,009,338 , RPL7L1, 20 more genes
    nsv4941132copy number variation1nstd200human GRCh38 chr6: 43,025,763-43,026,864 , GRCh37.p13 chr6: 42,993,501-42,994,602 RRP36
    nsv4934679copy number variation1nstd200human GRCh38 chr6: 43,022,141-43,022,905 , GRCh37.p13 chr6: 42,989,879-42,990,643 RRP36
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4592683copy number variation1nstd183human GRCh37 chr6: 42,627,455-43,357,404 , GRCh38.p12 chr6: 42,659,717-43,389,666 , PEX6, 36 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4141859copy number variation1nstd166human GRCh37.p13 chr6: 42,989,428-42,989,496 , GRCh38.p12 chr6: 43,021,690-43,021,758 KLHDC3, RRP36
    nsv3924318copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,336,296-44,558,281 , NCBI36 chr6: 42,444,274-44,666,259 , GRCh38 chr6: 42,368,558-44,590,544 MIR4642, SRF, 82 more genes
    nsv3919521copy number variation1nstd102humanPathogenic NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843 RPL23P6, LOC102723789, 184 more genes
    nsv3919402copy number variation1nstd102humanPathogenic NCBI36 chr6: 42,769,519-46,417,784 , GRCh37.p13 chr6: 42,661,541-46,309,825 , GRCh38.p12 chr6: 42,693,803-46,342,088 LOC101929770, MRPS18A, 94 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