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 376

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5598906copy number variation1nstd207human GRCh38 chr15: 28,350,984-28,351,256 , GRCh37.p13 chr15: 28,596,130-28,596,402 GOLGA6L24
    nsv5597933copy number variation1nstd207human GRCh38 chr15: 28,350,388-28,350,723 , GRCh37.p13 chr15: 28,595,534-28,595,869 GOLGA6L24
    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
    nsv5263684copy number variation1nstd204human GRCh38.p13 chr15: 28,357,701-28,358,500 , GRCh37.p13 chr15: 28,602,847-28,603,646 GOLGA6L24
    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
    nsv5060035copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,707,435-28,726,651 , GRCh38.p12 chr15: 23,462,288-28,481,505 PWAR4, SNORD116-18, 150 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
    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
    nsv4678824copy number variation1nstd190human GRCh37.p13 chr15: 22,781,807-29,006,030 , GRCh38.p12 chr15: 23,319,714-28,760,884 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 259 more genes
    nsv4678781copy number variation1nstd190human GRCh37.p13 chr15: 22,750,297-29,093,249 , GRCh38.p12 chr15: 23,319,714-28,848,103 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 259 more genes
    nsv4678780copy number variation1nstd190human GRCh37.p13 chr15: 22,750,297-28,539,834 , GRCh38.p12 chr15: 23,319,714-28,294,688 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 258 more genes
    nsv4678779copy number variation1nstd190human GRCh37.p13 chr15: 22,750,297-28,474,686 , GRCh38.p12 chr15: 23,319,714-28,229,540 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 258 more genes
    nsv4678747copy number variation1nstd190human GRCh37.p13 chr15: 22,567,553-28,539,834 , GRCh38.p12 chr15: 22,279,602-28,294,688 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 296 more genes
    nsv4678611copy number variation1nstd190human GRCh37.p13 chr15: 20,044,342-28,152,040 , GRCh38.p12 chr15: 19,839,089-27,906,894 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 395 more genes
    nsv4675913copy number variation1nstd102humanPathogenic GRCh37 chr15: 27,571,956-28,600,013 , GRCh38.p12 chr15: 27,326,809-28,354,867 , GRCh38.p12 chr15|NT_187660.1: 1-602,086 GABRG3, OCA2, 7 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