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 759

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5973840insertion1nstd209human GRCh38 chr18: 44,787,860-44,787,860 , GRCh37.p13 chr18: 42,367,825-42,367,825 SETBP1
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5941491copy number variation1nstd209human GRCh38 chr18: 44,715,283-44,715,593 , GRCh37.p13 chr18: 42,295,248-42,295,558 SETBP1
    nsv5937834copy number variation1nstd209human GRCh38 chr18: 44,740,255-44,740,310 , GRCh37.p13 chr18: 42,320,220-42,320,275 SETBP1
    nsv5928221copy number variation1nstd209human GRCh38 chr18: 45,045,451-45,046,132 , GRCh37.p13 chr18: 42,625,416-42,626,097 SETBP1
    nsv5887243copy number variation1nstd209human GRCh38 chr18: 44,743,226-44,745,685 , GRCh37.p13 chr18: 42,323,191-42,325,650 SETBP1
    nsv5878421copy number variation1nstd209human GRCh38 chr18: 45,031,849-45,034,548 , GRCh37.p13 chr18: 42,611,814-42,614,513 SETBP1
    nsv5730905mobile element insertion1nstd211human GRCh38 chr18: 44,885,510-44,885,510 , GRCh37.p13 chr18: 42,465,475-42,465,475 SETBP1
    nsv5723222mobile element insertion2nstd211human GRCh38 chr18: 44,914,925-44,914,925 , GRCh37.p13 chr18: 42,494,890-42,494,890 SETBP1
    nsv5714778mobile element insertion1nstd211human GRCh38 chr18: 44,976,413-44,976,413 , GRCh37.p13 chr18: 42,556,378-42,556,378 SETBP1
    nsv5711682mobile element insertion1nstd211human GRCh38 chr18: 44,999,986-44,999,986 , GRCh37.p13 chr18: 42,579,951-42,579,951 SETBP1
    nsv5704904mobile element insertion2nstd211human GRCh38 chr18: 45,032,528-45,032,528 , GRCh37.p13 chr18: 42,612,493-42,612,493 SETBP1
    nsv5696638mobile element insertion1nstd211human GRCh38 chr18: 44,792,960-44,792,960 , GRCh37.p13 chr18: 42,372,925-42,372,925 SETBP1
    nsv5656966insertion1nstd207human GRCh38 chr18: 44,721,942-44,721,942 , GRCh37.p13 chr18: 42,301,907-42,301,907 SETBP1
    nsv5584674copy number variation1nstd207human GRCh38 chr18: 45,045,451-45,046,132 , GRCh37.p13 chr18: 42,625,416-42,626,097 SETBP1
    nsv5554259mobile element insertion1nstd206human GRCh38 chr18: 44,914,925-44,914,976 , GRCh37.p13 chr18: 42,494,890-42,494,941 SETBP1
    nsv5533597copy number variation1nstd206human GRCh38 chr18: 44,892,539-44,894,740 , GRCh37.p13 chr18: 42,472,504-42,474,705 SETBP1
    nsv5527781copy number variation1nstd206human GRCh38 chr18: 45,045,451-45,046,134 , GRCh37.p13 chr18: 42,625,416-42,626,099 SETBP1
    nsv5522570copy number variation1nstd206human GRCh38 chr18: 44,921,052-44,921,102 , GRCh37.p13 chr18: 42,501,017-42,501,067 SETBP1
    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