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 223

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095026copy number variation2nstd102humanUncertain significance GRCh37 chr16: 49,525,186-51,631,253 , GRCh38.p12 chr16: 49,491,275-51,597,342 RNA5SP426, RPL34P29, 35 more genes
    nsv6997870copy number variation1nstd229human GRCh38 chr16: 50,567,683-50,567,724 , GRCh37.p13 chr16: 50,601,594-50,601,635 NKD1
    nsv6995316copy number variation1nstd229human GRCh38 chr16: 50,584,063-50,593,663 , GRCh37.p13 chr16: 50,617,974-50,627,574 NKD1
    nsv6992254copy number variation1nstd229human GRCh38 chr16: 50,591,997-50,597,740 , GRCh37.p13 chr16: 50,625,908-50,631,651 NKD1
    nsv6992192copy number variation1nstd229human GRCh38 chr16: 50,421,701-50,551,300 , GRCh37.p13 chr16: 50,455,612-50,585,211 NKD1
    nsv6991000copy number variation1nstd229human GRCh38 chr16: 50,578,326-50,590,177 , GRCh37.p13 chr16: 50,612,237-50,624,088 NKD1
    nsv6990953copy number variation1nstd229human GRCh38 chr16: 50,603,371-50,603,411 , GRCh37.p13 chr16: 50,637,282-50,637,322 NKD1
    nsv6988050copy number variation1nstd229human GRCh38 chr16: 50,561,864-50,566,913 , GRCh37.p13 chr16: 50,595,775-50,600,824 NKD1
    nsv6985683copy number variation1nstd229human GRCh38 chr16: 50,558,950-50,562,441 , GRCh37.p13 chr16: 50,592,861-50,596,352 NKD1
    nsv6983796copy number variation1nstd229human GRCh38 chr16: 50,574,655-50,579,743 , GRCh37.p13 chr16: 50,608,566-50,613,654 NKD1
    nsv6983132copy number variation1nstd229human GRCh38 chr16: 50,637,210-50,639,468 , GRCh37.p13 chr16: 50,671,121-50,673,379 NKD1
    nsv6981157copy number variation1nstd229human GRCh38 chr16: 50,593,613-50,596,523 , GRCh37.p13 chr16: 50,627,524-50,630,434 NKD1
    nsv6980353copy number variation1nstd229human GRCh38 chr16: 50,542,201-50,547,800 , GRCh37.p13 chr16: 50,576,112-50,581,711 NKD1
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6634436copy number variation1nstd102humanassociation GRCh37 chr16: 50,089,192-51,652,287 , GRCh38.p12 chr16: 50,055,281-51,618,376 CYLD-AS1, LOC107984892, 29 more genes
    nsv6501262copy number variation1nstd223human GRCh38 chr16: 50,593,613-50,596,521 , GRCh37.p13 chr16: 50,627,524-50,630,432 NKD1
    nsv6497263copy number variation1nstd223human GRCh38 chr16: 50,646,734-50,647,524 , GRCh37.p13 chr16: 50,680,645-50,681,435 NKD1
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6275346copy number variation1nstd214human GRCh38 chr16: 50,589,721-50,589,785 , GRCh37.p13 chr16: 50,623,632-50,623,696 NKD1
    nsv6229773insertion1nstd214human GRCh38 chr16: 50,579,168-50,579,168 , GRCh37.p13 chr16: 50,613,079-50,613,079 NKD1
    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