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 233

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115101mobile element insertion1nstd186human GRCh37 chr15: 80,197,648-80,197,699 , GRCh38.p12 chr15: 79,905,306-79,905,357 ST20, ST20-MTHFS
    nsv5979094inversion1nstd209human GRCh38 chr15: 79,905,293-79,905,599 , GRCh37.p13 chr15: 80,197,635-80,197,941 ST20, ST20-MTHFS
    nsv5940961copy number variation1nstd209human GRCh38 chr15: 79,909,871-79,909,925 , GRCh37.p13 chr15: 80,202,213-80,202,267 ST20-MTHFS, ST20
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5932262copy number variation1nstd209human GRCh38 chr15: 79,906,539-79,912,664 , GRCh37.p13 chr15: 80,198,881-80,205,006 ST20, ST20-MTHFS
    nsv5932196copy number variation1nstd209human GRCh38 chr15: 79,907,541-79,908,736 , GRCh37.p13 chr15: 80,199,883-80,201,078 ST20, ST20-MTHFS
    nsv5864492copy number variation1nstd209human GRCh38 chr15: 79,906,106-79,911,518 , GRCh37.p13 chr15: 80,198,448-80,203,860 ST20, ST20-MTHFS
    nsv5855682copy number variation1nstd209human GRCh38 chr15: 79,907,497-79,908,796 , GRCh37.p13 chr15: 80,199,839-80,201,138 ST20, ST20-MTHFS
    nsv5848515copy number variation1nstd209human GRCh38 chr15: 79,908,997-79,910,418 , GRCh37.p13 chr15: 80,201,339-80,202,760 ST20-MTHFS, ST20
    nsv5696699mobile element insertion2nstd211human GRCh38 chr15: 79,905,306-79,905,306 , GRCh37.p13 chr15: 80,197,648-80,197,648 ST20, ST20-MTHFS
    nsv5663444insertion1nstd207human GRCh38 chr15: 79,905,292-79,905,292 , GRCh37.p13 chr15: 80,197,634-80,197,634 ST20-MTHFS, ST20
    nsv5652609insertion1nstd207human GRCh38 chr15: 79,917,657-79,917,657 , GRCh37.p13 chr15: 80,209,999-80,209,999 ST20, ST20-MTHFS
    nsv5600224copy number variation1nstd207human GRCh38 chr15: 79,909,871-79,909,925 , GRCh37.p13 chr15: 80,202,213-80,202,267 ST20-MTHFS, ST20
    nsv5589965copy number variation1nstd207human GRCh38 chr15: 79,907,541-79,908,736 , GRCh37.p13 chr15: 80,199,883-80,201,078 ST20-MTHFS, ST20
    nsv5531188copy number variation1nstd206human GRCh38 chr15: 79,907,544-79,908,737 , GRCh37.p13 chr15: 80,199,886-80,201,079 ST20-MTHFS, ST20
    nsv5519371copy number variation1nstd206human GRCh38 chr15: 79,898,256-79,960,344 , GRCh37.p13 chr15: 80,190,598-80,252,686 BCL2A1, ST20-AS1, 3 more genes
    nsv5431096mobile element insertion1nstd206human GRCh38 chr15: 79,905,306-79,905,357 , GRCh37.p13 chr15: 80,197,648-80,197,699 ST20-MTHFS, ST20
    nsv5390522copy number variation1nstd186human GRCh37 chr15: 80,199,878-80,200,742 , GRCh38.p12 chr15: 79,907,536-79,908,400 ST20-MTHFS, ST20
    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
    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