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 118

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5864148copy number variation1nstd209human GRCh38 chr15: 68,264,147-68,281,371 , GRCh37.p13 chr15: 68,556,485-68,573,709 FEM1B
    nsv5646922insertion1nstd207human GRCh38 chr15: 68,286,870-68,286,870 , GRCh37.p13 chr15: 68,579,208-68,579,208 FEM1B
    nsv5541286insertion1nstd206human GRCh38 chr15: 68,281,489-68,281,528 , GRCh37.p13 chr15: 68,573,827-68,573,866 FEM1B
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv4992160copy number variation1nstd200human GRCh38 chr15: 68,273,713-68,277,695 , GRCh37.p13 chr15: 68,566,051-68,570,033 FEM1B
    nsv4849952copy number variation1nstd200human GRCh37 chr15: 68,566,051-68,570,033 , GRCh38.p12 chr15: 68,273,713-68,277,695 FEM1B
    nsv4546585insertion1nstd166human GRCh37.p13 chr15: 68,579,208-68,579,208 , GRCh38.p12 chr15: 68,286,870-68,286,870 FEM1B
    nsv4456268copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,369,118-70,481,307 , GRCh38.p12 chr15: 67,076,780-70,188,968 ANP32A-IT1, CARS1P1, 48 more genes
    nsv4236044copy number variation1nstd166human GRCh37.p13 chr15: 68,581,204-68,581,328 , GRCh38.p12 chr15: 68,288,866-68,288,990 FEM1B
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
    nsv3914011copy number variation1nstd102humanPathogenic NCBI36 chr15: 65,273,973-67,165,679 , GRCh37 chr15: 67,486,919-69,378,625 , GRCh38 chr15: 67,194,581-69,086,285 LOC105370871, IQCH-AS1, 29 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 MIR4513, LOC727751, 1754 more genes
    nsv3913103copy number variation1nstd102humanUncertain significance NCBI36 chr15: 64,381,145-66,377,062 , GRCh37.p13 chr15: 66,594,091-68,590,008 , GRCh38.p12 chr15: 66,301,753-68,297,670 IQCH, SMASR, 42 more genes
    nsv3913046copy number variation1nstd102humanLikely benign GRCh37 chr15: 68,226,097-69,058,832 , NCBI36 chr15: 66,013,151-66,845,886 , GRCh38 chr15: 67,933,759-68,766,493 LOC100286942, CLN6, 9 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