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 610

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124900insertion1nstd186human GRCh37 chr12: 71,081,117-71,081,146 , GRCh38.p12 chr12: 70,687,337-70,687,366 PTPRR
    nsv6114381mobile element insertion1nstd186human GRCh37 chr12: 71,152,218-71,152,269 , GRCh38.p12 chr12: 70,758,438-70,758,489 PTPRR
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5979282insertion1nstd209human GRCh38 chr12: 70,821,213-70,821,213 , GRCh37.p13 chr12: 71,214,993-71,214,993 PTPRR
    nsv5978890insertion1nstd209human GRCh38 chr12: 70,687,315-70,687,315 , GRCh37.p13 chr12: 71,081,095-71,081,095 PTPRR
    nsv5934041copy number variation1nstd209human GRCh38 chr12: 70,807,555-70,809,632 , GRCh37.p13 chr12: 71,201,335-71,203,412 PTPRR
    nsv5933722copy number variation1nstd209human GRCh38 chr12: 70,727,970-70,728,244 , GRCh37.p13 chr12: 71,121,750-71,122,024 PTPRR
    nsv5932363copy number variation1nstd209human GRCh38 chr12: 70,661,713-70,661,776 , GRCh37.p13 chr12: 71,055,493-71,055,556 PTPRR
    nsv5861085copy number variation1nstd209human GRCh38 chr12: 70,807,441-70,809,657 , GRCh37.p13 chr12: 71,201,221-71,203,437 PTPRR
    nsv5723052mobile element insertion1nstd211human GRCh38 chr12: 70,750,920-70,750,920 , GRCh37.p13 chr12: 71,144,700-71,144,700 PTPRR
    nsv5718491mobile element insertion2nstd211human GRCh38 chr12: 70,660,207-70,660,207 , GRCh37.p13 chr12: 71,053,987-71,053,987 PTPRR
    nsv5711471mobile element insertion2nstd211human GRCh38 chr12: 70,758,438-70,758,438 , GRCh37.p13 chr12: 71,152,218-71,152,218 PTPRR
    nsv5710060mobile element insertion2nstd211human GRCh38 chr12: 70,896,221-70,896,221 , GRCh37.p13 chr12: 71,290,001-71,290,001 PTPRR
    nsv5704413mobile element insertion1nstd211human GRCh38 chr12: 70,661,440-70,661,440 , GRCh37.p13 chr12: 71,055,220-71,055,220 PTPRR
    nsv5698898mobile element insertion2nstd211human GRCh38 chr12: 70,794,933-70,794,933 , GRCh37.p13 chr12: 71,188,713-71,188,713 PTPRR
    nsv5662869insertion1nstd207human GRCh38 chr12: 70,660,189-70,660,189 , GRCh37.p13 chr12: 71,053,969-71,053,969 PTPRR
    nsv5662320insertion1nstd207human GRCh38 chr12: 70,687,315-70,687,315 , GRCh37.p13 chr12: 71,081,095-71,081,095 PTPRR
    nsv5659239insertion1nstd207human GRCh38 chr12: 70,758,421-70,758,421 , GRCh37.p13 chr12: 71,152,201-71,152,201 PTPRR
    nsv5652881insertion1nstd207human GRCh38 chr12: 70,794,920-70,794,920 , GRCh37.p13 chr12: 71,188,700-71,188,700 PTPRR
    nsv5560176inversion1nstd206human GRCh38 chr12: 70,728,131-70,728,353 , GRCh37.p13 chr12: 71,121,911-71,122,133 PTPRR
    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