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 396

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094717copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,826,257-49,097,846 , GRCh38.p12 chr15: 48,534,060-48,805,649 FBN1, CEP152, 2 more genes
    nsv7072457inversion1nstd229human GRCh38 chr15: 48,724,104-48,724,278 , GRCh37.p13 chr15: 49,016,301-49,016,475 CEP152, LOC645405
    nsv7067502inversion1nstd229human GRCh38 chr15: 48,513,881-51,354,383 , GRCh37.p13 chr15: 48,806,078-51,646,580 NDUFAF4P1, MIR4713, 49 more genes
    nsv6976951copy number variation1nstd229human GRCh38 chr15: 48,696,401-48,722,100 , GRCh37.p13 chr15: 48,988,598-49,014,297 CEP152
    nsv6976429copy number variation1nstd229human GRCh38 chr15: 48,681,331-48,681,699 , GRCh37.p13 chr15: 48,973,528-48,973,896 CEP152
    nsv6973204copy number variation1nstd229human GRCh38 chr15: 48,708,901-48,714,500 , GRCh37.p13 chr15: 49,001,098-49,006,697 CEP152
    nsv6970215copy number variation1nstd229human GRCh38 chr15: 48,795,571-48,796,065 , GRCh37.p13 chr15: 49,087,768-49,088,262 CEP152
    nsv6968771copy number variation1nstd229human GRCh38 chr15: 48,771,078-48,838,415 , GRCh37.p13 chr15: 49,063,275-49,130,612 CEP152, SHC4
    nsv6968060copy number variation1nstd229human GRCh38 chr15: 48,682,394-48,688,875 , GRCh37.p13 chr15: 48,974,591-48,981,072 CEP152
    nsv6967488copy number variation1nstd229human GRCh38 chr15: 48,756,271-48,770,402 , GRCh37.p13 chr15: 49,048,468-49,062,599 CEP152
    nsv6964592copy number variation1nstd229human GRCh38 chr15: 48,652,301-48,722,100 , GRCh37.p13 chr15: 48,944,498-49,014,297 FBN1-DT, CEP152
    nsv6963955copy number variation1nstd229human GRCh38 chr15: 48,765,649-48,765,670 , GRCh37.p13 chr15: 49,057,846-49,057,867 CEP152
    nsv6963167copy number variation1nstd229human GRCh38 chr15: 48,762,801-48,766,800 , GRCh37.p13 chr15: 49,054,998-49,058,997 CEP152
    nsv6961948copy number variation1nstd229human GRCh38 chr15: 48,679,379-48,706,104 , GRCh37.p13 chr15: 48,971,576-48,998,301 CEP152
    nsv6960760copy number variation1nstd229human GRCh38 chr15: 48,702,912-48,703,288 , GRCh37.p13 chr15: 48,995,109-48,995,485 CEP152
    nsv6960418copy number variation1nstd229human GRCh38 chr15: 48,690,660-48,786,904 , GRCh37.p13 chr15: 48,982,857-49,079,101 LOC645405, CEP152
    nsv6959425copy number variation1nstd229human GRCh38 chr15: 48,697,604-48,705,404 , GRCh37.p13 chr15: 48,989,801-48,997,601 CEP152
    nsv6958782copy number variation1nstd229human GRCh38 chr15: 48,696,094-48,705,376 , GRCh37.p13 chr15: 48,988,291-48,997,573 CEP152
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6589696inversion1nstd223human GRCh38 chr15: 48,699,189-48,699,876 , GRCh37.p13 chr15: 48,991,386-48,992,073 CEP152
    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