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 211

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145212insertion1nstd232human GRCh37.p13 chr3: 160,143,988-160,143,988 , GRCh38.p12 chr3: 160,426,200-160,426,200 SMC4, TRIM59-IFT80
    nsv7141628insertion1nstd232human GRCh37.p13 chr3: 160,150,303-160,150,303 , GRCh38.p12 chr3: 160,432,515-160,432,515 SMC4, TRIM59-IFT80
    nsv7141553insertion1nstd232human GRCh37.p13 chr3: 160,130,244-160,130,244 , GRCh38.p12 chr3: 160,412,456-160,412,456 SMC4, TRIM59-IFT80
    nsv7140004insertion1nstd232human GRCh37.p13 chr3: 160,130,243-160,130,243 , GRCh38.p12 chr3: 160,412,455-160,412,455 SMC4, TRIM59-IFT80
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv7045413inversion1nstd229human GRCh38 chr3: 160,410,393-160,416,004 , GRCh37.p13 chr3: 160,128,181-160,133,792 TRIM59-IFT80, SMC4
    nsv6737487copy number variation1nstd229human GRCh38 chr3: 160,435,429-160,439,578 , GRCh37.p13 chr3: 160,153,217-160,157,366 TRIM59, SMC4, 1 more genes
    nsv6737233copy number variation1nstd229human GRCh38 chr3: 160,341,284-160,585,406 , GRCh37.p13 chr3: 160,059,072-160,303,194 MIR15B, B3GAT3P1, 11 more genes
    nsv6735288copy number variation1nstd229human GRCh38 chr3: 160,435,001-160,437,500 , GRCh37.p13 chr3: 160,152,789-160,155,288 TRIM59-IFT80, TRIM59, 1 more genes
    nsv6722572copy number variation1nstd229human GRCh38 chr3: 160,281,824-160,428,888 , GRCh37.p13 chr3: 159,999,612-160,146,676 MIR16-2, IFT80, 4 more genes
    nsv6721468copy number variation1nstd229human GRCh38 chr3: 160,395,969-160,399,053 , GRCh37.p13 chr3: 160,113,757-160,116,841 IFT80, SMC4, 1 more genes
    nsv6718522copy number variation1nstd229human GRCh38 chr3: 160,426,572-160,426,679 , GRCh37.p13 chr3: 160,144,360-160,144,467 TRIM59-IFT80, SMC4
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6563245inversion1nstd223human GRCh38 chr3: 160,421,067-160,421,474 , GRCh37.p13 chr3: 160,138,855-160,139,262 TRIM59-IFT80, SMC4
    nsv6358984copy number variation1nstd223human GRCh38 chr3: 160,395,997-160,399,027 , GRCh37.p13 chr3: 160,113,785-160,116,815 SMC4, IFT80, 1 more genes
    nsv6355919copy number variation1nstd223human GRCh38 chr3: 160,407,007-160,409,995 , GRCh37.p13 chr3: 160,124,795-160,127,783 SMC4, TRIM59-IFT80
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313664copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,768,935-160,158,553 , GRCh38.p12 chr3: 157,051,146-160,440,765 LOC105374179, RPL15P6, 49 more genes
    nsv6296203copy number variation1nstd186human GRCh37 chr3: 160,153,217-160,157,366 , GRCh38.p12 chr3: 160,435,429-160,439,578 SMC4, TRIM59, 1 more genes
    nsv6295815copy number variation1nstd186human GRCh37 chr3: 160,126,794-160,127,078 , GRCh38.p12 chr3: 160,409,006-160,409,290 TRIM59-IFT80, SMC4
    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