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 657

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969509insertion1nstd209human GRCh38 chr15: 59,209,813-59,209,813 , GRCh37.p13 chr15: 59,502,012-59,502,012 MYO1E
    nsv5968443insertion1nstd209human GRCh38 chr15: 59,268,720-59,268,720 , GRCh37.p13 chr15: 59,560,919-59,560,919 MYO1E
    nsv5968356insertion1nstd209human GRCh38 chr15: 59,253,901-59,253,901 , GRCh37.p13 chr15: 59,546,100-59,546,100 MYO1E
    nsv5947318copy number variation1nstd209human GRCh38 chr15: 59,213,439-59,213,728 , GRCh37.p13 chr15: 59,505,638-59,505,927 MYO1E
    nsv5944963copy number variation1nstd209human GRCh38 chr15: 59,317,963-59,389,505 , GRCh37.p13 chr15: 59,610,162-59,681,704 RNU6-212P, MYO1E
    nsv5929601copy number variation1nstd209human GRCh38 chr15: 59,228,897-59,229,045 , GRCh37.p13 chr15: 59,521,096-59,521,244 MYO1E
    nsv5866845copy number variation1nstd209human GRCh38 chr15: 59,317,955-59,340,524 , GRCh37.p13 chr15: 59,610,154-59,632,723 MYO1E, RNU6-212P
    nsv5866440copy number variation2nstd209human GRCh38 chr15: 59,323,399-59,324,498 , GRCh37.p13 chr15: 59,615,598-59,616,697 MYO1E
    nsv5858803copy number variation1nstd209human GRCh38 chr15: 59,326,324-59,333,823 , GRCh37.p13 chr15: 59,618,523-59,626,022 MYO1E
    nsv5850945copy number variation1nstd209human GRCh38 chr15: 59,371,077-59,372,486 , GRCh37.p13 chr15: 59,663,276-59,664,685 MYO1E
    nsv5713758mobile element insertion1nstd211human GRCh38 chr15: 59,338,301-59,338,301 , GRCh37.p13 chr15: 59,630,500-59,630,500 MYO1E
    nsv5707357mobile element insertion1nstd211human GRCh38 chr15: 59,367,021-59,367,021 , GRCh37.p13 chr15: 59,659,220-59,659,220 MYO1E
    nsv5706505mobile element insertion2nstd211human GRCh38 chr15: 59,310,672-59,310,672 , GRCh37.p13 chr15: 59,602,871-59,602,871 MYO1E
    nsv5664296insertion1nstd207human GRCh38 chr15: 59,282,928-59,282,928 , GRCh37.p13 chr15: 59,575,127-59,575,127 MYO1E
    nsv5648685insertion1nstd207human GRCh38 chr15: 59,314,808-59,314,808 , GRCh37.p13 chr15: 59,607,007-59,607,007 MYO1E
    nsv5561109sequence alteration1nstd206human GRCh38 chr15: 58,869,604-59,552,865 , GRCh37.p13 chr15: 59,161,803-59,845,064 MYO1E, RNF111, 14 more genes
    nsv5532827copy number variation1nstd206human GRCh38 chr15: 59,259,264-59,259,521 , GRCh37.p13 chr15: 59,551,463-59,551,720 MYO1E
    nsv5532094copy number variation1nstd206human GRCh38 chr15: 59,240,722-59,242,395 , GRCh37.p13 chr15: 59,532,921-59,534,594 MYO1E
    nsv5529823copy number variation1nstd206human GRCh38 chr15: 59,282,822-59,286,603 , GRCh37.p13 chr15: 59,575,021-59,578,802 MYO1E
    nsv5529703copy number variation1nstd206human GRCh38 chr15: 59,317,807-59,318,964 , GRCh37.p13 chr15: 59,610,006-59,611,163 MYO1E
    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