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 98

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5594743copy number variation1nstd207human GRCh38 chr11: 60,713,898-60,714,222 , GRCh37.p13 chr11: 60,481,371-60,481,695 MS4A8
    nsv5506160copy number variation1nstd206human GRCh38 chr11: 60,713,911-60,714,223 , GRCh37.p13 chr11: 60,481,384-60,481,696 MS4A8
    nsv5384967mobile element deletion1nstd186human GRCh37 chr11: 60,481,383-60,481,696 , GRCh38.p12 chr11: 60,713,910-60,714,223 MS4A8
    nsv5383322mobile element deletion1nstd186human GRCh37 chr11: 60,481,382-60,481,696 , GRCh38.p12 chr11: 60,713,909-60,714,223 MS4A8
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5355241translocation1nstd200human GRCh38 chr11: 60,706,556-60,706,556 , GRCh38 chr11: 60,706,372-60,706,372 , GRCh37.p13 chr11: 60,473,845-60,473,845 , GRCh37.p13 chr11: 60,474,029-60,474,029 MS4A8
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv5209213mobile element deletion1nstd204human GRCh38.p13 chr11: 60,713,881-60,714,252 , GRCh37.p13 chr11: 60,481,354-60,481,725 MS4A8
    nsv4979629copy number variation1nstd200human GRCh38 chr11: 60,702,517-60,704,253 , GRCh37.p13 chr11: 60,469,990-60,471,726 MS4A8, LOC105369321
    nsv4899677mobile element deletion1nstd200human GRCh38 chr11: 60,713,909-60,714,223 , GRCh37.p13 chr11: 60,481,382-60,481,696 MS4A8
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4774915mobile element deletion1nstd200human GRCh37 chr11: 60,481,383-60,481,696 , GRCh38.p12 chr11: 60,713,910-60,714,223 MS4A8
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4655506copy number variation1nstd186human GRCh37 chr11: 60,481,384-60,481,775 , GRCh38.p12 chr11: 60,713,911-60,714,302 MS4A8
    nsv4528891copy number variation1nstd166human GRCh37.p13 chr11: 60,481,384-60,481,775 , GRCh38.p12 chr11: 60,713,911-60,714,302 MS4A8
    nsv4489370mobile element insertion1nstd166human GRCh37.p13 chr11: 60,465,746-60,465,746 , GRCh38.p12 chr11: 60,698,273-60,698,273 MS4A8, LOC105369321
    nsv4382780copy number variation1nstd173human GRCh37 chr11: 60,408,412-60,465,698 , GRCh38.p12 chr11: 60,640,939-60,698,225 MS4A8, LOC105369321, 1 more genes
    nsv4197350copy number variation1nstd166human GRCh37.p13 chr11: 60,470,018-60,471,724 , GRCh38.p12 chr11: 60,702,545-60,704,251 LOC105369321, MS4A8
    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