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 493

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095847copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 108,604,612-109,579,739 , GRCh38.p12 chr2: 107,988,156-108,963,283 ACTP1, GCC2-AS1, 21 more genes
    nsv7046376inversion1nstd229human GRCh38 chr2: 106,214,512-108,776,331 , GRCh37.p13 chr2: 106,830,968-109,392,787 LOC107985931, LOC107985802, 42 more genes
    nsv7041064inversion1nstd229human GRCh38 chr2: 108,550,340-108,555,983 , GRCh37.p13 chr2: 109,166,796-109,172,439 LIMS1
    nsv7038094inversion1nstd229human GRCh38 chr2: 106,480,616-110,213,336 , GRCh37.p13 chr2: 107,097,072-110,970,913 WASF1P1, LOC105373985, 72 more genes
    nsv6696876copy number variation1nstd229human GRCh38 chr2: 108,635,501-108,638,891 , GRCh37.p13 chr2: 109,251,957-109,255,347 LIMS1
    nsv6695541copy number variation1nstd229human GRCh38 chr2: 108,558,196-108,564,076 , GRCh37.p13 chr2: 109,174,652-109,180,532 LIMS1
    nsv6694478copy number variation1nstd229human GRCh38 chr2: 108,672,196-108,672,221 , GRCh37.p13 chr2: 109,288,652-109,288,677 LIMS1
    nsv6693802copy number variation1nstd229human GRCh38 chr2: 108,623,725-108,624,116 , GRCh37.p13 chr2: 109,240,181-109,240,572 LIMS1
    nsv6691958copy number variation1nstd229human GRCh38 chr2: 108,610,897-108,621,402 , GRCh37.p13 chr2: 109,227,353-109,237,858 LIMS1
    nsv6689266copy number variation1nstd229human GRCh38 chr2: 108,420,201-108,560,000 , GRCh37.p13 chr2: 109,036,657-109,176,456 LIMS1, GCC2, 2 more genes
    nsv6688940copy number variation1nstd229human GRCh38 chr2: 108,591,296-108,595,229 , GRCh37.p13 chr2: 109,207,752-109,211,685 LIMS1
    nsv6688397copy number variation1nstd229human GRCh38 chr2: 108,608,582-108,610,328 , GRCh37.p13 chr2: 109,225,038-109,226,784 LIMS1
    nsv6686545copy number variation1nstd229human GRCh38 chr2: 103,585,907-110,943,040 , GRCh37.p13 chr2: 104,202,365-111,700,617 PPP1R2P5, CAPZBP1, 142 more genes
    nsv6686477copy number variation1nstd229human GRCh38 chr2: 108,610,901-108,623,400 , GRCh37.p13 chr2: 109,227,357-109,239,856 LIMS1
    nsv6686472copy number variation1nstd229human GRCh38 chr2: 108,580,928-108,641,193 , GRCh37.p13 chr2: 109,197,384-109,257,649 LIMS1
    nsv6685686copy number variation1nstd229human GRCh38 chr2: 108,630,530-108,630,611 , GRCh37.p13 chr2: 109,246,986-109,247,067 LIMS1
    nsv6684789copy number variation1nstd229human GRCh38 chr2: 108,618,247-108,632,648 , GRCh37.p13 chr2: 109,234,703-109,249,104 LIMS1
    nsv6679996copy number variation1nstd229human GRCh38 chr2: 108,596,005-108,599,518 , GRCh37.p13 chr2: 109,212,461-109,215,974 LIMS1
    nsv6678818copy number variation1nstd229human GRCh38 chr2: 108,628,786-108,632,364 , GRCh37.p13 chr2: 109,245,242-109,248,820 LIMS1
    nsv6678788copy number variation1nstd229human GRCh38 chr2: 108,631,215-108,636,169 , GRCh37.p13 chr2: 109,247,671-109,252,625 LIMS1
    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