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 344

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7094777copy number variation1nstd102humanPathogenic GRCh37 chr16: 27,441,393-29,001,333 , GRCh38.p12 chr16: 27,430,072-28,990,012 NUPR1, RPS15AP33, 45 more genes
    nsv7094776copy number variation1nstd102humanUncertain significance GRCh37 chr16: 27,441,393-28,899,063 , GRCh38.p12 chr16: 27,430,072-28,887,742 SH2B1, RNU6-1241P, 39 more genes
    nsv7076222inversion1nstd229human GRCh38 chr16: 28,418,032-28,817,928 , GRCh37.p13 chr16: 28,429,353-28,829,249 IL27, SULT1A2, 14 more genes
    nsv7070950inversion1nstd229human GRCh38 chr16: 28,377,390-28,737,947 , GRCh37.p13 chr16: 28,388,711-28,749,268 EIF3C, LOC107984835, 15 more genes
    nsv7066194inversion1nstd229human GRCh38 chr16: 28,508,623-28,616,440 , GRCh37.p13 chr16: 28,519,944-28,627,761 NUPR1, SGF29, 4 more genes
    nsv6989247copy number variation1nstd229human GRCh38 chr16: 28,543,501-28,561,600 , GRCh37.p13 chr16: 28,554,822-28,572,921 SGF29
    nsv6980690copy number variation1nstd229human GRCh38 chr16: 28,563,183-28,571,608 , GRCh37.p13 chr16: 28,574,504-28,582,929 SGF29
    nsv6979019copy number variation1nstd229human GRCh38 chr16: 28,572,787-28,576,433 , GRCh37.p13 chr16: 28,584,108-28,587,754 SGF29
    nsv6638016copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,486,929-29,351,826 , GRCh38.p12 chr16: 28,475,608-29,340,505 ATXN2L, LOC101928188, 33 more genes
    nsv6637786copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,384,464-29,432,245 , GRCh38.p12 chr16: 28,373,143-29,420,924 RABEP2, LOC105371159, 38 more genes
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637500copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,731-30,321,320 , GRCh38.p12 chr16: 28,455,410-30,309,999 CA5AP1, NPIPB13, 92 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6637294copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,490,480-29,379,768 , GRCh38.p12 chr16: 28,479,159-29,368,447 NPIPB9, CDC37P1, 33 more genes
    nsv6637171copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,371,468-29,342,589 , GRCh38.p12 chr16: 28,360,147-29,331,268 LOC105371159, IL27, 38 more genes
    nsv6634416copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,483,659-29,341,550 , GRCh38.p12 chr16: 28,472,338-29,330,229 LOC105371159, RPS15AP33, 33 more genes
    nsv6623197copy number variation2nstd224human GRCh37 chr16: 28,600,428-28,621,318 , GRCh38.p12 chr16: 28,589,107-28,609,997 SULT1A1, SGF29, 1 more genes
    nsv6580730inversion1nstd223human GRCh38 chr16: 28,562,815-28,563,913 , GRCh37.p13 chr16: 28,574,136-28,575,234 SGF29
    nsv6506788copy number variation1nstd223human GRCh38 chr16: 28,559,074-28,559,994 , GRCh37.p13 chr16: 28,570,395-28,571,315 SGF29
    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