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Items: 1 to 20 of 318

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139535copy number variation1nstd232human GRCh37.p13 chr16: 29,088,128-29,088,192 , GRCh38.p12 chr16: 29,076,807-29,076,871 RRN3P2
    nsv7071562inversion1nstd229human GRCh38 chr16: 29,034,709-29,294,722 , GRCh37.p13 chr16: 29,046,030-29,306,043 LOC101928188, LOC105371159, 5 more genes
    nsv6995374copy number variation1nstd229human GRCh38 chr16: 29,010,428-29,169,220 , GRCh37.p13 chr16: 29,021,749-29,180,541 RRN3P2, NPIPB10P, 2 more genes
    nsv6993988copy number variation1nstd229human GRCh38 chr16: 29,086,937-29,087,071 , GRCh37.p13 chr16: 29,098,258-29,098,392 RRN3P2
    nsv6990695copy number variation1nstd229human GRCh38 chr16: 29,115,006-29,118,987 , GRCh37.p13 chr16: 29,126,327-29,130,308 RRN3P2
    nsv6983661copy number variation1nstd229human GRCh38 chr16: 29,114,125-29,140,353 , GRCh37.p13 chr16: 29,125,446-29,151,674 RRN3P2, LOC100129184
    nsv6981356copy number variation1nstd229human GRCh38 chr16: 29,088,237-29,088,650 , GRCh37.p13 chr16: 29,099,558-29,099,971 RRN3P2
    nsv6978996copy number variation1nstd229human GRCh38 chr16: 29,102,101-29,106,600 , GRCh37.p13 chr16: 29,113,422-29,117,921 LOC101928215, RRN3P2
    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
    nsv6623637copy number variation1nstd224human GRCh37 chr16: 28,635,932-29,095,150 , GRCh38.p12 chr16: 28,624,611-29,083,829 EIF3C, SPNS1, 19 more genes
    nsv6505236copy number variation1nstd223human GRCh38 chr16: 29,067,828-29,077,366 , GRCh37.p13 chr16: 29,079,149-29,088,687 RRN3P2
    nsv6504214copy number variation1nstd223human GRCh38 chr16: 29,079,601-29,081,500 , GRCh37.p13 chr16: 29,090,922-29,092,821 RRN3P2
    nsv6315461copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,349,949-29,342,589 , GRCh38.p12 chr16: 28,338,628-29,331,268 CDC37P2, CDC37P1, 38 more genes
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