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 1831

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128563copy number variation1nstd186human GRCh37 chr22: 47,465,834-47,466,123 , GRCh38.p12 chr22: 47,069,938-47,070,227 TBC1D22A
    nsv6126123copy number variation1nstd186human GRCh37 chr22: 47,570,287-47,570,510 , GRCh38.p12 chr22: 47,174,644-47,174,867 TBC1D22A
    nsv6125855copy number variation1nstd186human GRCh37 chr22: 47,607,490-47,608,056 , GRCh38.p12 chr22: 47,211,740-47,212,306 TBC1D22A
    nsv6124839copy number variation1nstd186human GRCh37 chr22: 47,541,683-47,541,771 , GRCh38.p12 chr22: 47,146,040-47,146,128 TBC1D22A
    nsv6115743mobile element insertion1nstd186human GRCh37 chr22: 47,591,710-47,591,761 , GRCh38.p12 chr22: 47,195,960-47,196,011 TBC1D22A
    nsv6115453mobile element insertion1nstd186human GRCh37 chr22: 47,239,372-47,239,423 , GRCh38.p12 chr22: 46,843,475-46,843,526 TBC1D22A
    nsv6114333mobile element insertion1nstd186human GRCh37 chr22: 47,416,411-47,416,462 , GRCh38.p12 chr22: 47,020,515-47,020,566 TBC1D22A
    nsv5978037inversion1nstd209human GRCh38 chr22: 47,205,861-47,206,772 , GRCh37.p13 chr22: 47,601,611-47,602,522 TBC1D22A
    nsv5975821insertion1nstd209human GRCh38 chr22: 47,212,627-47,212,627 , GRCh37.p13 chr22: 47,608,377-47,608,377 TBC1D22A
    nsv5975592insertion1nstd209human GRCh38 chr22: 46,939,060-46,939,060 , GRCh37.p13 chr22: 47,334,956-47,334,956 TBC1D22A
    nsv5975443insertion1nstd209human GRCh38 chr22: 46,963,337-46,963,337 , GRCh37.p13 chr22: 47,359,233-47,359,233 TBC1D22A
    nsv5973204insertion1nstd209human GRCh38 chr22: 46,878,326-46,878,326 , GRCh37.p13 chr22: 47,274,222-47,274,222 TBC1D22A
    nsv5971754insertion1nstd209human GRCh38 chr22: 47,020,505-47,020,505 , GRCh37.p13 chr22: 47,416,401-47,416,401 TBC1D22A
    nsv5967186copy number variation1nstd209human GRCh38 chr22: 47,159,079-47,159,206 , GRCh37.p13 chr22: 47,554,722-47,554,849 TBC1D22A
    nsv5967017copy number variation1nstd209human GRCh38 chr22: 46,910,831-46,910,902 , GRCh37.p13 chr22: 47,306,727-47,306,798 TBC1D22A
    nsv5964947copy number variation1nstd209human GRCh38 chr22: 47,176,342-47,176,475 , GRCh37.p13 chr22: 47,572,006-47,572,227 TBC1D22A
    nsv5964937copy number variation1nstd209human GRCh38 chr22: 47,211,926-47,212,305 , GRCh37.p13 chr22: 47,607,676-47,608,055 TBC1D22A
    nsv5964534copy number variation1nstd209human GRCh38 chr22: 47,175,355-47,175,795 , GRCh37.p13 chr22: 47,570,998-47,571,438 TBC1D22A
    nsv5964259copy number variation1nstd209human GRCh38 chr22: 47,211,109-47,212,003 , GRCh37.p13 chr22: 47,606,859-47,607,753 TBC1D22A
    nsv5963703copy number variation1nstd209human GRCh38 chr22: 47,029,170-47,029,244 , GRCh37.p13 chr22: 47,425,066-47,425,140 TBC1D22A
    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