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 350

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971838inversion1nstd209human GRCh38 chr1: 52,869,986-52,997,049 , GRCh37.p13 chr1: 53,335,658-53,462,721 SCP2, ECHDC2, 6 more genes
    nsv5880630copy number variation1nstd209human GRCh38 chr1: 52,975,430-52,975,558 , GRCh37.p13 chr1: 53,441,102-53,441,230 SCP2
    nsv5872069copy number variation1nstd209human GRCh38 chr1: 52,951,381-52,954,090 , GRCh37.p13 chr1: 53,417,053-53,419,762 SCP2
    nsv5830059copy number variation1nstd209human GRCh38 chr1: 52,990,951-52,993,778 , GRCh37.p13 chr1: 53,456,623-53,459,450 RRAS2P1, SCP2, 1 more genes
    nsv5830058copy number variation1nstd209human GRCh38 chr1: 52,951,758-52,953,576 , GRCh37.p13 chr1: 53,417,430-53,419,248 SCP2
    nsv5678661mobile element insertion1nstd211human GRCh38 chr1: 52,930,073-52,930,073 , GRCh37.p13 chr1: 53,395,745-53,395,745 SCP2
    nsv5539690insertion1nstd206human GRCh38 chr1: 52,929,001-52,929,039 , GRCh37.p13 chr1: 53,394,673-53,394,711 SCP2
    nsv5433133copy number variation1nstd206human GRCh38 chr1: 52,955,151-52,958,248 , GRCh37.p13 chr1: 53,420,823-53,423,920 SCP2
    nsv5424885copy number variation1nstd206human GRCh38 chr1: 52,937,011-52,937,122 , GRCh37.p13 chr1: 53,402,683-53,402,794 SCP2
    nsv5424756copy number variation1nstd206human GRCh38 chr1: 53,020,241-53,021,297 , GRCh37.p13 chr1: 53,485,913-53,486,969 SCP2
    nsv5421833copy number variation1nstd206human GRCh38 chr1: 53,034,922-53,036,998 , GRCh37.p13 chr1: 53,500,594-53,502,670 SCP2
    nsv5417769copy number variation1nstd206human GRCh38 chr1: 52,957,963-52,959,908 , GRCh37.p13 chr1: 53,423,635-53,425,580 SCP2
    nsv5415189copy number variation1nstd206human GRCh38 chr1: 52,951,410-52,954,091 , GRCh37.p13 chr1: 53,417,082-53,419,763 SCP2
    nsv5397952mobile element insertion1nstd206human GRCh38 chr1: 52,930,073-52,930,124 , GRCh37.p13 chr1: 53,395,745-53,395,796 SCP2
    nsv5381135copy number variation1nstd102humanPathogenic GRCh37 chr1: 51,941,877-56,688,514 , GRCh38.p12 chr1: 51,476,205-56,222,842 LRP8-DT, LRRC42, 122 more genes
    nsv5291451copy number variation1nstd204human GRCh38.p13 chr1: 52,951,400-52,954,100 , GRCh37.p13 chr1: 53,417,072-53,419,772 SCP2
    nsv5209927copy number variation1nstd204human GRCh38.p13 chr1: 52,951,008-52,954,026 , GRCh37.p13 chr1: 53,416,680-53,419,698 SCP2
    nsv5201858copy number variation1nstd204human GRCh38.p13 chr1: 52,951,401-52,954,100 , GRCh37.p13 chr1: 53,417,073-53,419,772 SCP2
    nsv5185932mobile element insertion1nstd203human GRCh38 chr1: 52,986,226-52,986,242 , GRCh37.p13 chr1: 53,451,898-53,451,914 SCP2
    nsv5060193mobile element insertion1nstd203human GRCh38 chr1: 52,964,602-52,964,611 , GRCh37.p13 chr1: 53,430,274-53,430,283 SCP2
    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