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 178

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145558insertion1nstd232human GRCh37.p13 chr14: 67,841,267-67,841,267 , GRCh38.p12 chr14: 67,374,550-67,374,550 EIF2S1
    nsv7141638insertion1nstd232human GRCh37.p13 chr14: 67,831,727-67,831,727 , GRCh38.p12 chr14: 67,365,010-67,365,010 EIF2S1
    nsv7078008inversion1nstd229human GRCh38 chr14: 60,214,891-67,756,686 , GRCh37.p13 chr14: 60,681,609-68,223,403 ATP6V1D, LOC101927756, 129 more genes
    nsv7077538inversion1nstd229human GRCh38 chr14: 63,703,374-67,849,523 , GRCh37.p13 chr14: 64,170,092-68,316,240 RPPH1-2P, SYNE2, 75 more genes
    nsv7072917inversion1nstd229human GRCh38 chr14: 67,383,103-67,383,181 , GRCh37.p13 chr14: 67,849,820-67,849,898 EIF2S1
    nsv7068193inversion1nstd229human GRCh38 chr14: 65,793,880-70,322,609 , GRCh37.p13 chr14: 66,260,598-70,789,326 BANF1P1, GALNT16-AS1, 78 more genes
    nsv7058984inversion1nstd229human GRCh38 chr14: 65,563,947-68,493,504 , GRCh37.p13 chr14: 66,030,665-68,960,221 RN7SL108P, GPHN, 40 more genes
    nsv6969772copy number variation1nstd229human GRCh38 chr14: 67,359,401-67,361,000 , GRCh37.p13 chr14: 67,826,118-67,827,717 EIF2S1, ATP6V1D
    nsv6962517copy number variation1nstd229human GRCh38 chr14: 67,355,197-67,359,292 , GRCh37.p13 chr14: 67,821,914-67,826,009 ATP6V1D, EIF2S1
    nsv6962357copy number variation1nstd229human GRCh38 chr14: 67,320,493-67,377,743 , GRCh37.p13 chr14: 67,787,210-67,844,460 ATP6V1D, EIF2S1, 1 more genes
    nsv6961623copy number variation1nstd229human GRCh38 chr14: 67,333,364-67,372,117 , GRCh37.p13 chr14: 67,800,081-67,838,834 ATP6V1D, EIF2S1, 1 more genes
    nsv6958908copy number variation1nstd229human GRCh38 chr14: 67,052,720-67,475,133 , GRCh37.p13 chr14: 67,519,437-67,941,850 LOC105370538, GARIN2, 9 more genes
    nsv6591861inversion1nstd223human GRCh38 chr14: 65,793,878-70,322,614 , GRCh37.p13 chr14: 66,260,596-70,789,331 SLC8A3, GALNT16-AS1, 78 more genes
    nsv6587933inversion1nstd223human GRCh38 chr14: 67,367,471-67,367,619 , GRCh37.p13 chr14: 67,834,188-67,834,336 EIF2S1
    nsv6477512copy number variation1nstd223human GRCh38 chr14: 67,355,197-67,359,288 , GRCh37.p13 chr14: 67,821,914-67,826,005 EIF2S1, ATP6V1D
    nsv6476063copy number variation1nstd223human GRCh38 chr14: 64,354,345-74,200,229 , GRCh37.p13 chr14: 64,821,063-74,666,932 RNU6-240P, COX7A2P1, 196 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6314209copy number variation1nstd102humanUncertain significance GRCh37 chr14: 67,443,801-68,153,682 , GRCh38.p12 chr14: 66,977,084-67,686,965 PLEK2, EIF2S1, 18 more genes
    nsv6258987mobile element insertion1nstd215human GRCh38 chr14: 67,366,851-67,366,851 , GRCh37.p13 chr14: 67,833,568-67,833,568 EIF2S1
    nsv6123159copy number variation1nstd186human GRCh37 chr14: 67,834,192-67,834,322 , GRCh38.p12 chr14: 67,367,475-67,367,605 EIF2S1
    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