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 303

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980234inversion1nstd209human GRCh38 chr2: 130,052,690-131,284,721 , GRCh37.p13 chr2: 130,810,263-132,042,294 , PTPN18, 55 more genes
    nsv5968094inversion1nstd209human GRCh38 chr2: 130,018,896-131,305,572 , GRCh37.p13 chr2: 130,776,469-132,063,145 , PTPN18, 61 more genes
    nsv5893040copy number variation1nstd209human GRCh38 chr2: 131,062,472-131,062,668 , GRCh37.p13 chr2: 131,820,045-131,820,241 FAM168B
    nsv5891240copy number variation1nstd209human GRCh38 chr2: 131,086,782-131,087,100 , GRCh37.p13 chr2: 131,844,355-131,844,673 FAM168B
    nsv5677960mobile element insertion1nstd211human GRCh38 chr2: 131,063,317-131,063,317 , GRCh37.p13 chr2: 131,820,890-131,820,890 FAM168B
    nsv5665937inversion1nstd207human GRCh38 chr2: 130,138,213-131,531,319 , GRCh37.p13 chr2: 130,895,786-132,288,892 , GNAQP1, 84 more genes
    nsv5581489copy number variation1nstd207human GRCh38 chr2: 131,086,781-131,087,099 , GRCh37.p13 chr2: 131,844,354-131,844,672 FAM168B
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5453459copy number variation1nstd206human GRCh38 chr2: 131,074,003-131,074,098 , GRCh37.p13 chr2: 131,831,576-131,831,671 FAM168B
    nsv5452307copy number variation1nstd206human GRCh38 chr2: 131,091,624-131,092,066 , GRCh37.p13 chr2: 131,849,197-131,849,639 FAM168B
    nsv5447251copy number variation1nstd206human GRCh38 chr2: 131,087,465-131,088,220 , GRCh37.p13 chr2: 131,845,038-131,845,793 FAM168B
    nsv5445922copy number variation1nstd206human GRCh38 chr2: 131,062,472-131,062,673 , GRCh37.p13 chr2: 131,820,045-131,820,246 FAM168B
    nsv5441710copy number variation1nstd206human GRCh38 chr2: 131,060,525-131,066,246 , GRCh37.p13 chr2: 131,818,098-131,823,819 FAM168B
    nsv5439045copy number variation1nstd206human GRCh38 chr2: 131,086,782-131,087,083 , GRCh37.p13 chr2: 131,844,355-131,844,656 FAM168B
    nsv5382980mobile element deletion2nstd186human GRCh37 chr2: 131,844,355-131,844,656 , GRCh38.p12 chr2: 131,086,782-131,087,083 FAM168B
    nsv5327037inversion1nstd204human GRCh37.p13 chr2: 130,942,902-132,247,079 , GRCh38.p13 chr2: 130,185,329-131,489,506 , PTPN18, 79 more genes
    nsv5216632mobile element deletion1nstd204human GRCh38.p13 chr2: 131,086,782-131,087,083 , GRCh37.p13 chr2: 131,844,355-131,844,656 FAM168B
    nsv5037689inversion1nstd200human GRCh38 chr2: 130,226,386-131,459,405 , GRCh37.p13 chr2: 130,983,959-132,216,978 , MTND6P10, 73 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    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