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 220

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5966468insertion1nstd209human GRCh38 chr5: 39,292,867-39,292,867 , GRCh37.p13 chr5: 39,292,969-39,292,969 C9
    nsv5963052insertion1nstd209human GRCh38 chr5: 39,333,608-39,333,608 , GRCh37.p13 chr5: 39,333,710-39,333,710 C9
    nsv5893377copy number variation1nstd209human GRCh38 chr5: 39,313,603-39,313,868 , GRCh37.p13 chr5: 39,313,705-39,313,970 C9
    nsv5690066mobile element insertion2nstd211human GRCh38 chr5: 39,292,878-39,292,878 , GRCh37.p13 chr5: 39,292,980-39,292,980 C9
    nsv5678015mobile element insertion2nstd211human GRCh38 chr5: 39,336,848-39,336,848 , GRCh37.p13 chr5: 39,336,950-39,336,950 C9
    nsv5643758insertion1nstd207human GRCh38 chr5: 39,292,867-39,292,867 , GRCh37.p13 chr5: 39,292,969-39,292,969 C9
    nsv5640422insertion1nstd207human GRCh38 chr5: 39,333,608-39,333,608 , GRCh37.p13 chr5: 39,333,710-39,333,710 C9
    nsv5634101insertion1nstd207human GRCh38 chr5: 39,334,534-39,334,534 , GRCh37.p13 chr5: 39,334,636-39,334,636 C9
    nsv5629778insertion1nstd207human GRCh38 chr5: 39,336,848-39,336,848 , GRCh37.p13 chr5: 39,336,950-39,336,950 C9
    nsv5575380copy number variation1nstd207human GRCh38 chr5: 39,334,571-39,334,697 , GRCh37.p13 chr5: 39,334,673-39,334,799 C9
    nsv5538625insertion1nstd206human GRCh38 chr5: 39,336,848-39,336,848 , GRCh37.p13 chr5: 39,336,950-39,336,950 C9
    nsv5473520copy number variation1nstd206human GRCh38 chr5: 39,334,071-39,334,745 , GRCh37.p13 chr5: 39,334,173-39,334,847 C9
    nsv5473207copy number variation1nstd206human GRCh38 chr5: 39,300,480-39,300,605 , GRCh37.p13 chr5: 39,300,582-39,300,707 C9
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5467087copy number variation1nstd206human GRCh38 chr5: 39,334,790-39,339,317 , GRCh37.p13 chr5: 39,334,892-39,339,419 C9
    nsv5457847copy number variation1nstd206human GRCh38 chr5: 39,313,603-39,313,875 , GRCh37.p13 chr5: 39,313,705-39,313,977 C9
    nsv5455947copy number variation1nstd206human GRCh38 chr5: 39,323,019-39,324,789 , GRCh37.p13 chr5: 39,323,121-39,324,891 C9
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5368185translocation1nstd200human GRCh38 chr5: 39,324,789-39,324,789 , GRCh38 chr5: 39,323,019-39,323,019 , GRCh37.p13 chr5: 39,323,121-39,323,121 , GRCh37.p13 chr5: 39,324,891-39,324,891 C9
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center