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 648

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114903mobile element insertion1nstd186human GRCh37 chr20: 34,458,554-34,458,554 , GRCh38.p12 chr20: 35,870,632-35,870,632 PHF20
    nsv5980301insertion1nstd209human GRCh38 chr20: 35,829,527-35,829,527 , GRCh37.p13 chr20: 34,417,449-34,417,449 PHF20
    nsv5975048insertion1nstd209human GRCh38 chr20: 35,870,632-35,870,632 , GRCh37.p13 chr20: 34,458,554-34,458,554 PHF20
    nsv5963379copy number variation1nstd209human GRCh38 chr20: 35,889,977-35,890,277 , GRCh37.p13 chr20: 34,477,899-34,478,199 PHF20
    nsv5961095copy number variation1nstd209human GRCh38 chr20: 35,901,905-35,901,958 , GRCh37.p13 chr20: 34,489,827-34,489,880 PHF20
    nsv5960657copy number variation1nstd209human GRCh38 chr20: 35,906,443-35,906,534 , GRCh37.p13 chr20: 34,494,365-34,494,456 PHF20
    nsv5958395copy number variation1nstd209human GRCh38 chr20: 35,791,110-35,792,441 , GRCh37.p13 chr20: 34,379,032-34,380,363 PHF20
    nsv5954738copy number variation1nstd209human GRCh38 chr20: 35,787,729-35,788,493 , GRCh37.p13 chr20: 34,375,651-34,376,415 PHF20
    nsv5951765copy number variation1nstd209human GRCh38 chr20: 35,836,630-35,839,175 , GRCh37.p13 chr20: 34,424,552-34,427,097 PHF20
    nsv5886432copy number variation1nstd209human GRCh38 chr20: 35,836,717-35,838,916 , GRCh37.p13 chr20: 34,424,639-34,426,838 PHF20
    nsv5872524copy number variation1nstd209human GRCh38 chr20: 35,791,339-35,792,670 , GRCh37.p13 chr20: 34,379,261-34,380,592 PHF20
    nsv5723033mobile element insertion2nstd211human GRCh38 chr20: 35,829,541-35,829,541 , GRCh37.p13 chr20: 34,417,463-34,417,463 PHF20
    nsv5710816mobile element insertion2nstd211human GRCh38 chr20: 35,824,149-35,824,149 , GRCh37.p13 chr20: 34,412,071-34,412,071 PHF20
    nsv5709804mobile element insertion1nstd211human GRCh38 chr20: 35,885,500-35,885,500 , GRCh37.p13 chr20: 34,473,422-34,473,422 PHF20
    nsv5706084mobile element insertion2nstd211human GRCh38 chr20: 35,870,644-35,870,644 , GRCh37.p13 chr20: 34,458,566-34,458,566 PHF20
    nsv5669316insertion1nstd207human GRCh38 chr20: 35,870,632-35,870,632 , GRCh37.p13 chr20: 34,458,554-34,458,554 PHF20
    nsv5668088insertion1nstd207human GRCh38 chr20: 35,928,297-35,928,297 , GRCh37.p13 chr20: 34,516,219-34,516,219 PHF20, RNU6-937P
    nsv5598113copy number variation1nstd207human GRCh38 chr20: 35,906,443-35,906,534 , GRCh37.p13 chr20: 34,494,365-34,494,456 PHF20
    nsv5597950copy number variation1nstd207human GRCh38 chr20: 35,901,905-35,901,958 , GRCh37.p13 chr20: 34,489,827-34,489,880 PHF20
    nsv5596324copy number variation1nstd207human GRCh38 chr20: 35,850,576-35,850,626 , GRCh37.p13 chr20: 34,438,498-34,438,548 PHF20, COX7BP2
    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