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 1184

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143560insertion1nstd232human GRCh37.p13 chr2: 42,833,190-42,833,190 , GRCh38.p12 chr2: 42,606,050-42,606,050 MTA3, LOC105374555
    nsv7139029insertion1nstd232human GRCh37.p13 chr2: 42,832,781-42,832,781 , GRCh38.p12 chr2: 42,605,641-42,605,641 MTA3, LOC105374555
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7056543inversion1nstd229human GRCh38 chr2: 42,536,211-42,556,650 , GRCh37.p13 chr2: 42,763,351-42,783,790 MTA3
    nsv7053944inversion1nstd229human GRCh38 chr2: 42,575,192-42,575,301 , GRCh37.p13 chr2: 42,802,332-42,802,441 MTA3
    nsv7047281inversion1nstd229human GRCh38 chr2: 42,508,678-42,508,729 , GRCh37.p13 chr2: 42,735,818-42,735,869 MTA3
    nsv7041290inversion1nstd229human GRCh38 chr2: 41,299,652-42,501,090 , GRCh37.p13 chr2: 41,526,792-42,728,230 RPS13P3, EML4-AS1, 15 more genes
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv7039614inversion1nstd229human GRCh38 chr2: 42,524,155-42,524,180 , GRCh37.p13 chr2: 42,751,295-42,751,320 MTA3
    nsv6675912copy number variation1nstd229human GRCh38 chr2: 42,509,010-42,593,952 , GRCh37.p13 chr2: 42,736,150-42,821,092 MTA3, LOC105374555
    nsv6675851copy number variation1nstd229human GRCh38 chr2: 42,730,201-42,737,400 , GRCh37.p13 chr2: 42,957,341-42,964,540 MTA3
    nsv6675559copy number variation1nstd229human GRCh38 chr2: 42,748,565-42,748,702 , GRCh37.p13 chr2: 42,975,705-42,975,842 MTA3
    nsv6675359copy number variation1nstd229human GRCh38 chr2: 42,724,970-42,730,875 , GRCh37.p13 chr2: 42,952,110-42,958,015 MTA3
    nsv6675094copy number variation1nstd229human GRCh38 chr2: 42,710,579-42,711,290 , GRCh37.p13 chr2: 42,937,719-42,938,430 RNU6-137P, MTA3
    nsv6674315copy number variation1nstd229human GRCh38 chr2: 42,759,749-42,761,217 , GRCh37.p13 chr2: 42,986,889-42,988,357 OXER1, MTA3
    nsv6673997copy number variation1nstd229human GRCh38 chr2: 42,766,516-42,773,041 , GRCh37.p13 chr2: 42,993,656-43,000,181 MTA3, HAAO
    nsv6673502copy number variation1nstd229human GRCh38 chr2: 42,415,701-42,721,700 , GRCh37.p13 chr2: 42,642,841-42,948,840 VDAC1P13, MTA3, 4 more genes
    nsv6672145copy number variation1nstd229human GRCh38 chr2: 42,392,538-42,558,773 , GRCh37.p13 chr2: 42,619,678-42,785,913 RPS13P3, KCNG3, 2 more genes
    nsv6671944copy number variation1nstd229human GRCh38 chr2: 42,767,697-42,770,216 , GRCh37.p13 chr2: 42,994,837-42,997,356 MTA3, HAAO
    nsv6671006copy number variation1nstd229human GRCh38 chr2: 42,740,464-42,741,028 , GRCh37.p13 chr2: 42,967,604-42,968,168 MTA3
    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