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 377

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5930400copy number variation1nstd209human GRCh38 chr15: 28,463,398-28,585,449 , GRCh37.p13 chr15: 28,708,544-28,830,595 GOLGA8G, GOLGA6L25, 6 more genes
    nsv5672660copy number variation1nstd102humanPathogenic GRCh38 chr15: 22,804,175-30,375,696 , GRCh37.p13 chr15: 23,564,855-30,667,899 TUBBP8, LOC102723564, 218 more genes
    nsv5671633inversion1nstd207human GRCh38 chr15: 28,298,425-28,623,514 , GRCh37.p13 chr15: 28,543,571-28,868,660 HERC2P1, HERC2, 16 more genes
    nsv5496896copy number variation1nstd206human GRCh38 chr15: 28,172,874-28,679,000 , GRCh37.p13 chr15: 28,418,020-28,924,146 MIR4509-3, LOC100419574, 18 more genes
    nsv5277039copy number variation1nstd204human GRCh38.p13 chr15: 28,515,701-28,521,600 , GRCh37.p13 chr15: 28,760,847-28,766,746 GOLGA8G
    nsv5274113copy number variation1nstd204human GRCh38.p13 chr15: 28,526,101-28,526,600 , GRCh37.p13 chr15: 28,771,247-28,771,746 GOLGA8G
    nsv5272896copy number variation1nstd204human GRCh38.p13 chr15: 28,513,101-28,521,600 , GRCh37.p13 chr15: 28,758,247-28,766,746 GOLGA8G
    nsv5272547copy number variation1nstd204human GRCh38.p13 chr15: 28,531,001-28,531,700 , GRCh37.p13 chr15: 28,776,147-28,776,846 GOLGA8G
    nsv5269083copy number variation1nstd204human GRCh38.p13 chr15: 28,512,501-28,517,800 , GRCh37.p13 chr15: 28,757,647-28,762,946 GOLGA8G
    nsv5269060copy number variation1nstd204human GRCh38.p13 chr15: 28,521,601-28,522,100 , GRCh37.p13 chr15: 28,766,747-28,767,246 GOLGA8G
    nsv5267780copy number variation1nstd204human GRCh38.p13 chr15: 28,522,501-28,530,200 , GRCh37.p13 chr15: 28,767,647-28,775,346 GOLGA8G
    nsv5260546copy number variation1nstd204human GRCh38.p13 chr15: 28,518,001-28,530,200 , GRCh37.p13 chr15: 28,763,147-28,775,346 GOLGA8G
    nsv5200367copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,208,842-28,525,460 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,280,314 SNORD115-27, LOC105370747, 246 more genes
    nsv4729149copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 28,709,714-34,506,805 , GRCh38.p12 chr15: 28,464,568-34,214,604 APBA2, CHRM5, 125 more genes
    nsv4685685copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,646,692-28,964,445 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,719,299 MKRN3, RN7SL469P, 247 more genes
    nsv4685661copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,416-28,566,671 , GRCh38.p12 chr15: 23,319,714-28,321,525 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC101060587, MPHOSPH10P8, 246 more genes
    nsv4684444copy number variation1nstd192human GRCh38.p12 chr15: 23,319,714-28,097,771 , GRCh37 chr15: 22,927,167-28,342,917 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 258 more genes
    nsv4680125copy number variation1nstd189human GRCh37.p13 chr15: 28,443,911-29,330,792 , GRCh38.p12 chr15: 28,198,765-29,038,589 , GRCh38.p12 chr15|NT_187660.1: 486,810-1,313,540 , GRCh38.p12 chr15|NW_011332701.1: 332,206-1,201,056 APBA2, HERC2P1, 29 more genes
    nsv4679328copy number variation1nstd189human GRCh37.p13 chr15: 28,751,724-30,478,655 , GRCh38.p12 chr15: 28,506,578-30,186,452 , GRCh38.p12 chr15|NT_187660.1: 782,375-2,471,400 , GRCh38.p12 chr15|NW_011332701.1: 668,589-2,358,916 APBA2, TJP1, 37 more genes
    nsv4678889copy number variation1nstd189human GRCh37.p13 chr15: 28,536,237-31,026,703 , GRCh38.p12 chr15: 28,291,091-30,734,500 , APBA2, 71 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