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 718

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967543insertion1nstd209human GRCh38 chr1: 113,478,472-113,478,472 , GRCh37.p13 chr1: 114,021,094-114,021,094 MAGI3
    nsv5961739insertion1nstd209human GRCh38 chr1: 113,545,882-113,545,882 , GRCh37.p13 chr1: 114,088,504-114,088,504 MAGI3
    nsv5948273insertion1nstd209human GRCh38 chr1: 113,497,219-113,497,219 , GRCh37.p13 chr1: 114,039,841-114,039,841 MAGI3
    nsv5883270copy number variation1nstd209human GRCh38 chr1: 113,632,820-113,636,174 , GRCh37.p13 chr1: 114,175,442-114,178,796 MAGI3
    nsv5879077copy number variation1nstd209human GRCh38 chr1: 113,517,694-113,519,669 , GRCh37.p13 chr1: 114,060,316-114,062,291 MAGI3
    nsv5871897copy number variation1nstd209human GRCh38 chr1: 113,530,751-113,530,804 , GRCh37.p13 chr1: 114,073,373-114,073,426 MAGI3
    nsv5870114copy number variation1nstd209human GRCh38 chr1: 113,549,861-113,550,152 , GRCh37.p13 chr1: 114,092,483-114,092,774 MAGI3
    nsv5868590copy number variation1nstd209human GRCh38 chr1: 113,415,985-113,416,078 , GRCh37.p13 chr1: 113,958,607-113,958,700 MAGI3
    nsv5868389copy number variation1nstd209human GRCh38 chr1: 113,550,238-113,553,837 , GRCh37.p13 chr1: 114,092,860-114,096,459 MAGI3
    nsv5827812copy number variation1nstd209human GRCh38 chr1: 113,515,732-113,517,281 , GRCh37.p13 chr1: 114,058,354-114,059,903 MAGI3
    nsv5827726copy number variation1nstd209human GRCh38 chr1: 113,550,649-113,553,969 , GRCh37.p13 chr1: 114,093,271-114,096,591 MAGI3
    nsv5827613copy number variation1nstd209human GRCh38 chr1: 113,632,968-113,636,049 , GRCh37.p13 chr1: 114,175,590-114,178,671 MAGI3
    nsv5827611copy number variation1nstd209human GRCh38 chr1: 113,517,732-113,519,669 , GRCh37.p13 chr1: 114,060,354-114,062,291 MAGI3
    nsv5730315mobile element insertion2nstd211human GRCh38 chr1: 113,503,748-113,503,748 , GRCh37.p13 chr1: 114,046,370-114,046,370 MAGI3
    nsv5729985mobile element insertion2nstd211human GRCh38 chr1: 113,633,279-113,633,279 , GRCh37.p13 chr1: 114,175,901-114,175,901 MAGI3
    nsv5715146mobile element insertion2nstd211human GRCh38 chr1: 113,545,899-113,545,899 , GRCh37.p13 chr1: 114,088,521-114,088,521 MAGI3
    nsv5715027mobile element insertion1nstd211human GRCh38 chr1: 113,609,898-113,609,898 , GRCh37.p13 chr1: 114,152,520-114,152,520 MAGI3
    nsv5693875mobile element insertion1nstd211human GRCh38 chr1: 113,661,819-113,661,819 , GRCh37.p13 chr1: 114,204,441-114,204,441 MAGI3
    nsv5692857mobile element insertion1nstd211human GRCh38 chr1: 113,462,826-113,462,826 , GRCh37.p13 chr1: 114,005,448-114,005,448 MAGI3
    nsv5687564mobile element insertion1nstd211human GRCh38 chr1: 113,648,623-113,648,623 , GRCh37.p13 chr1: 114,191,245-114,191,245 MAGI3
    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