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 518

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120615copy number variation1nstd186human GRCh37 chr16: 746,678-746,734 , GRCh38.p12 chr16: 696,678-696,734 FBXL16
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5933970copy number variation1nstd209human GRCh38 chr16: 691,758-692,048 , GRCh37.p13 chr16: 741,758-742,048 FBXL16
    nsv5706044mobile element insertion1nstd211human GRCh38 chr16: 692,506-692,506 , GRCh37.p13 chr16: 742,506-742,506 FBXL16
    nsv5658399insertion1nstd207human GRCh38 chr16: 696,678-696,678 , GRCh37.p13 chr16: 746,678-746,678 FBXL16
    nsv5651534insertion1nstd207human GRCh38 chr16: 707,613-707,613 , GRCh37.p13 chr16: 757,613-757,613 FBXL16
    nsv5604203copy number variation1nstd207human GRCh38 chr16: 707,559-707,762 , GRCh37.p13 chr16: 757,559-757,762 FBXL16
    nsv5597404copy number variation1nstd207human GRCh38 chr16: 707,559-707,626 , GRCh37.p13 chr16: 757,559-757,626 FBXL16
    nsv5531462copy number variation1nstd206human GRCh38 chr16: 696,678-696,734 , GRCh37.p13 chr16: 746,678-746,734 FBXL16
    nsv5524136copy number variation1nstd206human GRCh38 chr16: 694,769-694,851 , GRCh37.p13 chr16: 744,769-744,851 FBXL16
    nsv5423736mobile element insertion1nstd206human GRCh38 chr16: 692,506-692,557 , GRCh37.p13 chr16: 742,506-742,557 FBXL16
    nsv5380998copy number variation2nstd102humanUncertain significance GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915 NDUFB10, BAIAP3, 102 more genes
    nsv5279314copy number variation1nstd204human GRCh38.p13 chr16: 631,501-737,100 , GRCh37.p13 chr16: 681,501-787,100 , CIAO3, 18 more genes
    nsv5278593copy number variation1nstd204human GRCh38.p13 chr16: 495,101-1,599,500 , GRCh37.p13 chr16: 545,101-1,649,501 , MIR662, 73 more genes
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv5264761copy number variation1nstd204human GRCh38.p13 chr16: 701,330-702,329 , GRCh37.p13 chr16: 751,330-752,329 FBXL16
    nsv5263615copy number variation1nstd204human GRCh38.p13 chr16: 504,601-857,400 , GRCh37.p13 chr16: 554,601-907,400 , LINC00235, 36 more genes
    nsv4759002insertion1nstd199human GRCh37 chr16: 746,680-746,680 , GRCh38.p12 chr16: 696,680-696,680 FBXL16
    nsv4748142copy number variation1nstd199human GRCh37 chr16: 757,581-757,650 , GRCh38.p12 chr16: 707,581-707,650 FBXL16
    nsv4731970copy number variation1nstd199human GRCh37 chr16: 741,657-741,952 , GRCh38.p12 chr16: 691,657-691,952 FBXL16
    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