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 1146

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6119238copy number variation1nstd186human GRCh37 chr1: 60,048,974-60,049,661 , GRCh38.p12 chr1: 59,583,302-59,583,989 FGGY
    nsv5963138insertion1nstd209human GRCh38 chr1: 59,360,105-59,360,105 , GRCh37.p13 chr1: 59,825,777-59,825,777 FGGY
    nsv5954958insertion1nstd209human GRCh38 chr1: 59,721,337-59,721,337 , GRCh37.p13 chr1: 60,187,009-60,187,009 FGGY
    nsv5954510insertion1nstd209human GRCh38 chr1: 59,491,041-59,491,041 , GRCh37.p13 chr1: 59,956,713-59,956,713 FGGY
    nsv5953848insertion1nstd209human GRCh38 chr1: 59,337,048-59,337,048 , GRCh37.p13 chr1: 59,802,720-59,802,720 FGGY
    nsv5953764insertion1nstd209human GRCh38 chr1: 59,406,190-59,406,190 , GRCh37.p13 chr1: 59,871,862-59,871,862 FGGY
    nsv5887138copy number variation1nstd209human GRCh38 chr1: 59,531,384-59,589,482 , GRCh37.p13 chr1: 59,997,056-60,055,154 FGGY
    nsv5886179copy number variation1nstd209human GRCh38 chr1: 59,584,685-59,591,037 , GRCh37.p13 chr1: 60,050,357-60,056,709 FGGY
    nsv5885752copy number variation1nstd209human GRCh38 chr1: 59,581,052-59,584,963 , GRCh37.p13 chr1: 60,046,724-60,050,635 FGGY
    nsv5884415copy number variation1nstd209human GRCh38 chr1: 59,582,964-59,583,988 , GRCh37.p13 chr1: 60,048,636-60,049,660 FGGY
    nsv5874011copy number variation1nstd209human GRCh38 chr1: 59,327,352-59,327,465 , GRCh37.p13 chr1: 59,793,024-59,793,137 FGGY
    nsv5871676copy number variation1nstd209human GRCh38 chr1: 59,617,887-59,618,003 , GRCh37.p13 chr1: 60,083,559-60,083,675 FGGY
    nsv5871490copy number variation1nstd209human GRCh38 chr1: 59,640,572-59,641,422 , GRCh37.p13 chr1: 60,106,244-60,107,094 FGGY
    nsv5869981copy number variation1nstd209human GRCh38 chr1: 59,612,042-59,615,835 , GRCh37.p13 chr1: 60,077,714-60,081,507 FGGY
    nsv5869171copy number variation1nstd209human GRCh38 chr1: 59,377,108-59,377,239 , GRCh37.p13 chr1: 59,842,780-59,842,911 FGGY
    nsv5867962copy number variation1nstd209human GRCh38 chr1: 59,507,994-59,614,821 , GRCh37.p13 chr1: 59,973,666-60,080,493 FGGY
    nsv5830410copy number variation1nstd209human GRCh38 chr1: 59,581,013-59,583,012 , GRCh37.p13 chr1: 60,046,685-60,048,684 FGGY
    nsv5830409copy number variation1nstd209human GRCh38 chr1: 59,507,995-59,547,872 , GRCh37.p13 chr1: 59,973,667-60,013,544 FGGY
    nsv5830385copy number variation2nstd209human GRCh38 chr1: 59,585,691-59,595,904 , GRCh37.p13 chr1: 60,051,363-60,061,576 FGGY
    nsv5830384copy number variation1nstd209human GRCh38 chr1: 59,584,423-59,610,967 , GRCh37.p13 chr1: 60,050,095-60,076,639 FGGY
    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