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 178

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5829827copy number variation1nstd209human GRCh38 chr1: 28,749,310-28,752,559 , GRCh37.p13 chr1: 29,075,822-29,079,071 YTHDF2
    nsv5829826copy number variation1nstd209human GRCh38 chr1: 28,738,703-28,739,802 , GRCh37.p13 chr1: 29,065,215-29,066,314 YTHDF2
    nsv5560510sequence alteration1nstd206human GRCh38 chr1: 28,760,609-28,761,650 , GRCh37.p13 chr1: 29,087,121-29,088,162 YTHDF2
    nsv5559232inversion1nstd206human GRCh38 chr1: 28,760,589-28,761,325 , GRCh37.p13 chr1: 29,087,101-29,087,837 YTHDF2
    nsv5433141copy number variation1nstd206human GRCh38 chr1: 28,752,582-28,753,942 , GRCh37.p13 chr1: 29,079,094-29,080,454 YTHDF2
    nsv5428962copy number variation1nstd206human GRCh38 chr1: 28,760,453-28,763,025 , GRCh37.p13 chr1: 29,086,965-29,089,537 YTHDF2
    nsv5350664translocation1nstd200human GRCh38 chr9: 24,721,647-24,721,647 , GRCh38 chr1: 28,769,065-28,769,065 , GRCh37.p13 chr1: 29,095,577-29,095,577 , GRCh37.p13 chr9: 24,721,645-24,721,645 YTHDF2
    nsv5335959translocation1nstd200human GRCh37 chr9: 24,721,645-24,721,645 , GRCh37 chr1: 29,095,577-29,095,577 , GRCh38.p12 chr1: 28,769,065-28,769,065 , GRCh38.p12 chr9: 24,721,647-24,721,647 YTHDF2
    nsv5212241copy number variation1nstd204human GRCh38.p13 chr1: 28,084,401-28,971,400 , GRCh37.p13 chr1: 28,410,912-29,297,912 SNORA73B, ARL8BP2, 29 more genes
    nsv5075934mobile element insertion1nstd203human GRCh38 chr1: 28,753,358-28,753,398 , GRCh37.p13 chr1: 29,079,870-29,079,910 YTHDF2
    nsv5075811mobile element insertion1nstd203human GRCh38 chr1: 28,753,398-28,753,398 , GRCh37.p13 chr1: 29,079,910-29,079,910 YTHDF2
    nsv5074146mobile element insertion1nstd203human GRCh38 chr1: 28,753,366-28,753,398 , GRCh37.p13 chr1: 29,079,878-29,079,910 YTHDF2
    nsv5069332mobile element insertion1nstd203human GRCh38 chr1: 28,753,227-28,753,240 , GRCh37.p13 chr1: 29,079,739-29,079,752 YTHDF2
    nsv5065528mobile element insertion1nstd203human GRCh38 chr1: 28,754,179-28,754,196 , GRCh37.p13 chr1: 29,080,691-29,080,708 YTHDF2
    nsv5061387mobile element insertion1nstd203human GRCh38 chr1: 28,753,364-28,753,398 , GRCh37.p13 chr1: 29,079,876-29,079,910 YTHDF2
    nsv4895656copy number variation1nstd200human GRCh38 chr1: 28,767,067-28,767,735 , GRCh37.p13 chr1: 29,093,579-29,094,247 YTHDF2
    nsv4895655copy number variation1nstd200human GRCh38 chr1: 28,761,699-28,768,091 , GRCh37.p13 chr1: 29,088,211-29,094,603 YTHDF2
    nsv4895654copy number variation1nstd200human GRCh38 chr1: 28,759,092-28,759,147 , GRCh37.p13 chr1: 29,085,604-29,085,659 YTHDF2
    nsv4895653copy number variation1nstd200human GRCh38 chr1: 28,757,701-28,758,776 , GRCh37.p13 chr1: 29,084,213-29,085,288 YTHDF2
    nsv4895652copy number variation1nstd200human GRCh38 chr1: 28,752,928-28,755,342 , GRCh37.p13 chr1: 29,079,440-29,081,854 YTHDF2
    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