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 352

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966769insertion1nstd209human GRCh38 chr6: 158,566,478-158,566,478 , GRCh37.p13 chr6: 158,987,510-158,987,510 TMEM181
    nsv5960605insertion1nstd209human GRCh38 chr6: 158,605,126-158,605,126 , GRCh37.p13 chr6: 159,026,158-159,026,158 TMEM181
    nsv5907076copy number variation1nstd209human GRCh38 chr6: 158,595,303-158,597,317 , GRCh37.p13 chr6: 159,016,335-159,018,349 TMEM181
    nsv5903970copy number variation1nstd209human GRCh38 chr6: 158,579,060-158,580,131 , GRCh37.p13 chr6: 159,000,092-159,001,163 TMEM181
    nsv5903623copy number variation1nstd209human GRCh38 chr6: 158,571,365-158,571,430 , GRCh37.p13 chr6: 158,992,397-158,992,462 TMEM181
    nsv5896526copy number variation1nstd209human GRCh38 chr6: 158,571,376-158,571,577 , GRCh37.p13 chr6: 158,992,408-158,992,609 TMEM181
    nsv5895094copy number variation1nstd209human GRCh38 chr6: 158,572,848-158,572,915 , GRCh37.p13 chr6: 158,993,880-158,993,947 TMEM181
    nsv5890116copy number variation1nstd209human GRCh38 chr6: 158,566,478-158,566,558 , GRCh37.p13 chr6: 158,987,510-158,987,590 TMEM181
    nsv5844684copy number variation1nstd209human GRCh38 chr6: 158,595,307-158,597,406 , GRCh37.p13 chr6: 159,016,339-159,018,438 TMEM181
    nsv5844149copy number variation1nstd209human GRCh38 chr6: 158,579,107-158,580,106 , GRCh37.p13 chr6: 159,000,139-159,001,138 TMEM181
    nsv5678744mobile element insertion1nstd211human GRCh38 chr6: 158,601,830-158,601,830 , GRCh37.p13 chr6: 159,022,862-159,022,862 TMEM181
    nsv5641129insertion1nstd207human GRCh38 chr6: 158,606,281-158,606,281 , GRCh37.p13 chr6: 159,027,313-159,027,313 TMEM181
    nsv5627752insertion1nstd207human GRCh38 chr6: 158,566,552-158,566,552 , GRCh37.p13 chr6: 158,987,584-158,987,584 TMEM181
    nsv5580728copy number variation1nstd207human GRCh38 chr6: 158,571,365-158,571,430 , GRCh37.p13 chr6: 158,992,397-158,992,462 TMEM181
    nsv5573212copy number variation1nstd207human GRCh38 chr6: 158,571,376-158,571,577 , GRCh37.p13 chr6: 158,992,408-158,992,609 TMEM181
    nsv5471626copy number variation1nstd206human GRCh38 chr6: 158,634,580-158,636,088 , GRCh37.p13 chr6: 159,055,612-159,057,120 TMEM181, DYNLT1
    nsv5466747copy number variation1nstd206human GRCh38 chr6: 158,570,488-158,571,343 , GRCh37.p13 chr6: 158,991,520-158,992,375 TMEM181
    nsv5402923mobile element insertion1nstd206human GRCh38 chr6: 158,601,830-158,601,881 , GRCh37.p13 chr6: 159,022,862-159,022,913 TMEM181
    nsv5386490copy number variation2nstd186human GRCh37 chr6: 158,992,292-158,992,613 , GRCh38.p12 chr6: 158,571,260-158,571,581 TMEM181
    nsv5363500translocation1nstd200human GRCh38 chr6: 158,571,482-158,571,482 , GRCh38 chr6: 158,570,510-158,570,510 , GRCh37.p13 chr6: 158,992,514-158,992,514 , GRCh37.p13 chr6: 158,991,542-158,991,542 TMEM181
    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