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 831

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5979532inversion1nstd209human GRCh38 chr4: 4,147,913-9,493,295 , GRCh37.p13 chr4: 4,149,640-9,494,939 , CRMP1, 130 more genes
    nsv5974394inversion1nstd209human GRCh38 chr4: 4,005,086-9,639,734 , GRCh37.p13 chr4: 4,006,813-9,641,358 , CRMP1, 142 more genes
    nsv5973087inversion1nstd209human GRCh38 chr4: 3,883,398-8,956,544 , GRCh37.p13 chr4: 3,885,125-8,958,270 , CRMP1, 102 more genes
    nsv5959974insertion1nstd209human GRCh38 chr4: 6,462,482-6,462,482 , GRCh37.p13 chr4: 6,464,209-6,464,209 PPP2R2C
    nsv5953296insertion1nstd209human GRCh38 chr4: 6,397,539-6,397,539 , GRCh37.p13 chr4: 6,399,266-6,399,266 PPP2R2C
    nsv5905273copy number variation1nstd209human GRCh38 chr4: 6,490,399-6,496,471 , GRCh37.p13 chr4: 6,492,126-6,498,198 PPP2R2C
    nsv5902032copy number variation1nstd209human GRCh38 chr4: 6,336,660-6,336,847 , GRCh37.p13 chr4: 6,338,387-6,338,574 PPP2R2C
    nsv5901908copy number variation1nstd209human GRCh38 chr4: 6,420,263-6,421,780 , GRCh37.p13 chr4: 6,421,990-6,423,507 PPP2R2C
    nsv5897521copy number variation1nstd209human GRCh38 chr4: 6,396,834-6,396,934 , GRCh37.p13 chr4: 6,398,561-6,398,661 PPP2R2C
    nsv5895184copy number variation1nstd209human GRCh38 chr4: 6,410,932-6,411,615 , GRCh37.p13 chr4: 6,412,659-6,413,342 PPP2R2C
    nsv5894259copy number variation1nstd209human GRCh38 chr4: 6,546,616-6,558,496 , GRCh37.p13 chr4: 6,548,343-6,560,223 PPP2R2C
    nsv5891831copy number variation1nstd209human GRCh38 chr4: 6,329,569-6,329,640 , GRCh37.p13 chr4: 6,331,296-6,331,367 PPP2R2C
    nsv5840075copy number variation1nstd209human GRCh38 chr4: 6,546,627-6,558,222 , GRCh37.p13 chr4: 6,548,354-6,559,949 PPP2R2C
    nsv5840070copy number variation1nstd209human GRCh38 chr4: 6,420,301-6,421,800 , GRCh37.p13 chr4: 6,422,028-6,423,527 PPP2R2C
    nsv5839753copy number variation1nstd209human GRCh38 chr4: 6,490,437-6,492,436 , GRCh37.p13 chr4: 6,492,164-6,494,163 PPP2R2C
    nsv5720743mobile element insertion1nstd211human GRCh38 chr4: 6,449,081-6,449,081 , GRCh37.p13 chr4: 6,450,808-6,450,808 PPP2R2C
    nsv5682292mobile element insertion1nstd211human GRCh38 chr4: 6,444,128-6,444,128 , GRCh37.p13 chr4: 6,445,855-6,445,855 PPP2R2C
    nsv5680490mobile element insertion1nstd211human GRCh38 chr4: 6,327,763-6,327,763 , GRCh37.p13 chr4: 6,329,490-6,329,490 PPP2R2C
    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