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 106

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5698940mobile element insertion1nstd211human GRCh38 chr19: 57,445,399-57,445,399 , GRCh37.p13 chr19: 57,956,767-57,956,767 ZNF749
    nsv5525116copy number variation1nstd206human GRCh38 chr19: 57,437,647-57,442,111 , GRCh37.p13 chr19: 57,949,015-57,953,479 ZNF749
    nsv5520651copy number variation1nstd206human GRCh38 chr19: 57,447,560-57,448,574 , GRCh37.p13 chr19: 57,958,928-57,959,942 ZNF749
    nsv5518084copy number variation1nstd206human GRCh38 chr19: 57,441,919-57,442,054 , GRCh37.p13 chr19: 57,953,287-57,953,422 ZNF749
    nsv5418919mobile element insertion1nstd206human GRCh38 chr19: 57,445,399-57,445,450 , GRCh37.p13 chr19: 57,956,767-57,956,818 ZNF749
    nsv5292903copy number variation1nstd204human GRCh38.p13 chr19: 57,172,601-57,751,900 , GRCh37.p13 chr19: 57,683,969-58,263,268 TPRG1LP1, ZNF805, 30 more genes
    nsv5028194copy number variation1nstd200human GRCh38 chr19: 57,437,572-57,442,111 , GRCh37.p13 chr19: 57,948,940-57,953,479 ZNF749
    nsv5025006copy number variation1nstd200human GRCh38 chr19: 57,404,109-57,438,820 , GRCh37.p13 chr19: 57,915,477-57,950,188 ZNF749, ZNF17
    nsv4865375copy number variation1nstd200human GRCh37 chr19: 57,915,477-57,950,188 , GRCh38.p12 chr19: 57,404,109-57,438,820 ZNF17, ZNF749
    nsv4861499copy number variation1nstd200human GRCh37 chr19: 57,948,940-57,953,480 , GRCh38.p12 chr19: 57,437,572-57,442,112 ZNF749
    nsv4775446mobile element deletion1nstd200human GRCh37 chr19: 57,943,191-57,943,497 , GRCh38.p12 chr19: 57,431,823-57,432,129 ZNF749
    nsv4751796insertion1nstd199human GRCh37 chr19: 57,946,582-57,946,582 , GRCh38.p12 chr19: 57,435,214-57,435,214 ZNF749
    nsv4457732copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,952,073-58,661,581 , GRCh38.p12 chr19: 57,440,705-58,150,214 ZNF418, ZNF606-AS1, 39 more genes
    nsv4271159copy number variation1nstd166human GRCh37.p13 chr19: 57,945,399-57,958,118 , GRCh38.p12 chr19: 57,434,031-57,446,750 ZNF749
    nsv4270637copy number variation1nstd166human GRCh37.p13 chr19: 57,951,541-57,951,669 , GRCh38.p12 chr19: 57,440,173-57,440,301 ZNF749
    nsv3956291copy number variation1nstd168human GRCh38 chr19: 57,430,294-57,488,538 , GRCh37.p13 chr19: 57,941,662-57,999,906 ZNF419, ZNF749, 3 more genes
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 RPL39P37, CCDC106, 556 more genes
    nsv3923909copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203 OSCAR, FKBP1AP1, 535 more genes
    nsv3923613copy number variation1nstd102humanPathogenic GRCh38 chr19: 52,612,432-58,581,203 , GRCh37 chr19: 53,115,685-59,092,570 , NCBI36 chr19: 57,807,497-63,784,382 ZNF71-SMIM17, MIR518E, 393 more genes
    nsv3922599copy number variation1nstd102humanPathogenic GRCh38 chr19: 51,141,518-58,539,965 , NCBI36 chr19: 56,336,587-63,743,144 , GRCh37 chr19: 51,644,775-59,051,332 LOC100421130, A1BG-AS1, 475 more genes
    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