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 1086

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131216insertion1nstd186human GRCh37 chr17: 55,616,992-55,616,992 , GRCh38.p12 chr17: 57,539,631-57,539,631 MSI2
    nsv5972720insertion1nstd209human GRCh38 chr17: 57,583,488-57,583,488 , GRCh37.p13 chr17: 55,660,849-55,660,849 MSI2
    nsv5972097insertion1nstd209human GRCh38 chr17: 57,539,630-57,539,630 , GRCh37.p13 chr17: 55,616,991-55,616,991 MSI2
    nsv5971054insertion1nstd209human GRCh38 chr17: 57,410,008-57,410,008 , GRCh37.p13 chr17: 55,487,369-55,487,369 MSI2
    nsv5947253copy number variation1nstd209human GRCh38 chr17: 57,509,673-57,510,679 , GRCh37.p13 chr17: 55,587,034-55,588,040 MSI2
    nsv5940266copy number variation1nstd209human GRCh38 chr17: 57,617,037-57,618,900 , GRCh37.p13 chr17: 55,694,398-55,696,261 RN7SL449P, MSI2
    nsv5939680copy number variation1nstd209human GRCh38 chr17: 57,610,448-57,612,552 , GRCh37.p13 chr17: 55,687,809-55,689,913 MSI2
    nsv5939299copy number variation1nstd209human GRCh38 chr17: 57,437,712-57,437,821 , GRCh37.p13 chr17: 55,515,073-55,515,182 MSI2
    nsv5938107copy number variation1nstd209human GRCh38 chr17: 57,649,228-57,649,444 , GRCh37.p13 chr17: 55,726,589-55,726,805 MSI2
    nsv5936177copy number variation1nstd209human GRCh38 chr17: 57,533,660-57,533,822 , GRCh37.p13 chr17: 55,611,021-55,611,183 MSI2
    nsv5935775copy number variation1nstd209human GRCh38 chr17: 57,374,513-57,374,649 , GRCh37.p13 chr17: 55,451,874-55,452,010 MSI2
    nsv5932977copy number variation1nstd209human GRCh38 chr17: 57,413,340-57,414,141 , GRCh37.p13 chr17: 55,490,701-55,491,502 MSI2
    nsv5931557copy number variation1nstd209human GRCh38 chr17: 57,422,257-57,422,711 , GRCh37.p13 chr17: 55,499,618-55,500,072 MSI2
    nsv5929393copy number variation1nstd209human GRCh38 chr17: 57,464,351-57,465,421 , GRCh37.p13 chr17: 55,541,712-55,542,782 MSI2
    nsv5881380copy number variation1nstd209human GRCh38 chr17: 57,610,464-57,612,585 , GRCh37.p13 chr17: 55,687,825-55,689,946 MSI2
    nsv5868728copy number variation1nstd209human GRCh38 chr17: 57,464,407-57,465,406 , GRCh37.p13 chr17: 55,541,768-55,542,767 MSI2
    nsv5712663mobile element insertion1nstd211human GRCh38 chr17: 57,450,255-57,450,255 , GRCh37.p13 chr17: 55,527,616-55,527,616 MSI2
    nsv5705462mobile element insertion2nstd211human GRCh38 chr17: 57,390,385-57,390,385 , GRCh37.p13 chr17: 55,467,746-55,467,746 MSI2
    nsv5703922mobile element insertion2nstd211human GRCh38 chr17: 57,360,868-57,360,868 , GRCh37.p13 chr17: 55,438,229-55,438,229 MSI2
    nsv5699923mobile element insertion1nstd211human GRCh38 chr17: 57,284,629-57,284,629 , GRCh37.p13 chr17: 55,361,990-55,361,990 MSI2
    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