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 378

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938581copy number variation1nstd209human GRCh38 chr16: 11,589,877-11,591,437 , GRCh37.p13 chr16: 11,683,733-11,685,293 LITAF
    nsv5928737copy number variation1nstd209human GRCh38 chr16: 11,614,447-11,617,631 , GRCh37.p13 chr16: 11,708,303-11,711,487 LITAF
    nsv5878728copy number variation1nstd209human GRCh38 chr16: 11,589,874-11,591,473 , GRCh37.p13 chr16: 11,683,730-11,685,329 LITAF
    nsv5876425copy number variation1nstd209human GRCh38 chr16: 11,614,491-11,617,240 , GRCh37.p13 chr16: 11,708,347-11,711,096 LITAF
    nsv5712952mobile element insertion1nstd211human GRCh38 chr16: 11,588,701-11,588,701 , GRCh37.p13 chr16: 11,682,557-11,682,557 LITAF
    nsv5649383insertion1nstd207human GRCh38 chr16: 11,616,531-11,616,531 , GRCh37.p13 chr16: 11,710,387-11,710,387 LITAF
    nsv5597767copy number variation1nstd207human GRCh38 chr16: 11,589,877-11,591,437 , GRCh37.p13 chr16: 11,683,733-11,685,293 LITAF
    nsv5530138copy number variation1nstd206human GRCh38 chr16: 11,615,042-11,615,156 , GRCh37.p13 chr16: 11,708,898-11,709,012 LITAF
    nsv5528043copy number variation1nstd206human GRCh38 chr16: 11,589,903-11,591,438 , GRCh37.p13 chr16: 11,683,759-11,685,294 LITAF
    nsv5524656copy number variation1nstd206human GRCh38 chr16: 11,567,146-11,568,104 , GRCh37.p13 chr16: 11,661,002-11,661,960 LITAF
    nsv5524364copy number variation1nstd206human GRCh38 chr16: 11,592,908-11,595,467 , GRCh37.p13 chr16: 11,686,764-11,689,323 LITAF
    nsv5521125copy number variation1nstd206human GRCh38 chr16: 11,619,627-11,626,384 , GRCh37.p13 chr16: 11,713,483-11,720,240 , LITAF
    nsv5516026copy number variation1nstd206human GRCh38 chr16: 11,580,371-11,641,790 , GRCh37.p13 chr16: 11,674,227-11,735,646 , LITAF
    nsv5426257mobile element insertion1nstd206human GRCh38 chr16: 11,588,701-11,588,752 , GRCh37.p13 chr16: 11,682,557-11,682,608 LITAF
    nsv5380990copy number variation1nstd102humanUncertain significance GRCh37 chr16: 11,650,347-11,650,606 , GRCh38.p12 chr16: 11,556,491-11,556,750 LITAF
    nsv5365520translocation1nstd200human GRCh38 chr16: 11,568,746-11,568,746 , GRCh38 chr16: 11,577,522-11,577,522 , GRCh37.p13 chr16: 11,662,602-11,662,602 , GRCh37.p13 chr16: 11,671,378-11,671,378 LITAF
    nsv5365519translocation1nstd200human GRCh38 chr16: 11,567,523-11,567,523 , GRCh38 chr16: 11,572,670-11,572,670 , GRCh37.p13 chr16: 11,661,379-11,661,379 , GRCh37.p13 chr16: 11,666,526-11,666,526 LITAF
    nsv5334095translocation1nstd200human GRCh37 chr16: 11,662,602-11,662,602 , GRCh37 chr16: 11,671,378-11,671,378 , GRCh38.p12 chr16: 11,568,746-11,568,746 , GRCh38.p12 chr16: 11,577,522-11,577,522 LITAF
    nsv5330986translocation1nstd200human GRCh37 chr16: 11,661,332-11,661,332 , GRCh37 chr16: 11,661,410-11,661,410 , GRCh38.p12 chr16: 11,567,476-11,567,476 , GRCh38.p12 chr16: 11,567,554-11,567,554 LITAF
    nsv5303344copy number variation1nstd204human GRCh38.p13 chr16: 11,589,903-11,591,438 , GRCh37.p13 chr16: 11,683,759-11,685,294 LITAF
    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