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 656

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098884copy number variation1nstd102humanPathogenic GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093 LOC105377879, LOC100421583, 47 more genes
    nsv7055788inversion1nstd229human GRCh38 chr6: 83,387,431-83,393,127 , GRCh37.p13 chr6: 84,097,150-84,102,846 ME1
    nsv7041924inversion1nstd229human GRCh38 chr6: 83,352,412-83,356,091 , GRCh37.p13 chr6: 84,062,131-84,065,810 ME1
    nsv7040466inversion1nstd229human GRCh38 chr6: 83,380,781-83,386,377 , GRCh37.p13 chr6: 84,090,500-84,096,096 ME1
    nsv7040331inversion1nstd229human GRCh38 chr6: 83,392,875-83,393,058 , GRCh37.p13 chr6: 84,102,594-84,102,777 ME1
    nsv7039395inversion1nstd229human GRCh38 chr6: 83,383,861-83,384,010 , GRCh37.p13 chr6: 84,093,580-84,093,729 ME1
    nsv6818048copy number variation1nstd229human GRCh38 chr6: 83,317,357-83,317,456 , GRCh37.p13 chr6: 84,027,076-84,027,175 ME1
    nsv6816854copy number variation1nstd229human GRCh38 chr6: 83,298,441-83,971,760 , GRCh37.p13 chr6: 84,008,160-84,681,479 RIPPLY2, ME1, 4 more genes
    nsv6816427copy number variation1nstd229human GRCh38 chr6: 83,304,158-83,312,000 , GRCh37.p13 chr6: 84,013,877-84,021,719 ME1
    nsv6815757copy number variation1nstd229human GRCh38 chr6: 83,223,723-83,226,792 , GRCh37.p13 chr6: 83,933,442-83,936,511 ME1
    nsv6814357copy number variation1nstd229human GRCh38 chr6: 83,247,692-83,329,277 , GRCh37.p13 chr6: 83,957,411-84,038,996 ME1
    nsv6814176copy number variation1nstd229human GRCh38 chr6: 83,407,258-83,407,812 , GRCh37.p13 chr6: 84,116,977-84,117,531 ME1
    nsv6812006copy number variation1nstd229human GRCh38 chr6: 83,418,635-83,426,273 , GRCh37.p13 chr6: 84,128,354-84,135,992 ME1
    nsv6811354copy number variation1nstd229human GRCh38 chr6: 83,371,871-83,375,778 , GRCh37.p13 chr6: 84,081,590-84,085,497 ME1
    nsv6809782copy number variation1nstd229human GRCh38 chr6: 83,240,101-83,241,800 , GRCh37.p13 chr6: 83,949,820-83,951,519 ME1
    nsv6808469copy number variation1nstd229human GRCh38 chr6: 83,270,882-83,270,938 , GRCh37.p13 chr6: 83,980,601-83,980,657 ME1
    nsv6808085copy number variation1nstd229human GRCh38 chr6: 83,350,302-83,356,377 , GRCh37.p13 chr6: 84,060,021-84,066,096 ME1
    nsv6807974copy number variation1nstd229human GRCh38 chr6: 83,215,958-83,227,377 , GRCh37.p13 chr6: 83,925,677-83,937,096 ME1
    nsv6807620copy number variation1nstd229human GRCh38 chr6: 83,272,992-83,276,588 , GRCh37.p13 chr6: 83,982,711-83,986,307 ME1
    nsv6807606copy number variation1nstd229human GRCh38 chr6: 83,228,651-83,249,100 , GRCh37.p13 chr6: 83,938,370-83,958,819 ME1
    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