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 684

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112837mobile element insertion1nstd186human GRCh37 chr20: 50,349,198-50,349,249 , GRCh38.p12 chr20: 51,732,659-51,732,710 ATP9A, LOC100419570
    nsv5967987insertion1nstd209human GRCh38 chr20: 51,732,647-51,732,647 , GRCh37.p13 chr20: 50,349,186-50,349,186 ATP9A, LOC100419570
    nsv5962203copy number variation1nstd209human GRCh38 chr20: 51,740,439-51,740,559 , GRCh37.p13 chr20: 50,356,978-50,357,098 ATP9A
    nsv5960386copy number variation1nstd209human GRCh38 chr20: 51,746,416-51,746,556 , GRCh37.p13 chr20: 50,362,955-50,363,095 ATP9A
    nsv5950936copy number variation1nstd209human GRCh38 chr20: 51,650,511-51,651,667 , GRCh37.p13 chr20: 50,267,050-50,268,206 ATP9A
    nsv5713739mobile element insertion2nstd211human GRCh38 chr20: 51,732,659-51,732,659 , GRCh37.p13 chr20: 50,349,198-50,349,198 LOC100419570, ATP9A
    nsv5700471mobile element insertion2nstd211human GRCh38 chr20: 51,597,599-51,597,599 , GRCh37.p13 chr20: 50,214,138-50,214,138 ATP9A
    nsv5671981insertion1nstd207human GRCh38 chr20: 51,651,255-51,651,255 , GRCh37.p13 chr20: 50,267,794-50,267,794 ATP9A
    nsv5669137insertion1nstd207human GRCh38 chr20: 51,740,560-51,740,560 , GRCh37.p13 chr20: 50,357,099-50,357,099 ATP9A
    nsv5668008insertion1nstd207human GRCh38 chr20: 51,635,822-51,635,822 , GRCh37.p13 chr20: 50,252,361-50,252,361 ATP9A
    nsv5664745insertion1nstd207human GRCh38 chr20: 51,732,647-51,732,647 , GRCh37.p13 chr20: 50,349,186-50,349,186 ATP9A, LOC100419570
    nsv5536004insertion1nstd206human GRCh38 chr20: 51,650,512-51,650,512 , GRCh37.p13 chr20: 50,267,051-50,267,051 ATP9A
    nsv5531666copy number variation1nstd206human GRCh38 chr20: 51,651,668-51,651,921 , GRCh37.p13 chr20: 50,268,207-50,268,460 ATP9A
    nsv5527769copy number variation1nstd206human GRCh38 chr20: 51,755,877-51,760,711 , GRCh37.p13 chr20: 50,372,416-50,377,250 ATP9A
    nsv5525789copy number variation1nstd206human GRCh38 chr20: 51,671,346-51,674,035 , GRCh37.p13 chr20: 50,287,885-50,290,574 ATP9A
    nsv5518964copy number variation1nstd206human GRCh38 chr20: 51,753,351-51,753,430 , GRCh37.p13 chr20: 50,369,890-50,369,969 ATP9A
    nsv5517657copy number variation1nstd206human GRCh38 chr20: 51,707,255-51,709,623 , GRCh37.p13 chr20: 50,323,794-50,326,162 ATP9A
    nsv5516948copy number variation1nstd206human GRCh38 chr20: 51,738,160-51,753,810 , GRCh37.p13 chr20: 50,354,699-50,370,349 ATP9A
    nsv5514119copy number variation1nstd206human GRCh38 chr20: 51,738,799-51,740,066 , GRCh37.p13 chr20: 50,355,338-50,356,605 ATP9A
    nsv5422710mobile element insertion1nstd206human GRCh38 chr20: 51,597,599-51,597,650 , GRCh37.p13 chr20: 50,214,138-50,214,189 ATP9A
    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