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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942043copy number variation1nstd209human GRCh38 chr19: 1,021,960-1,037,278 , GRCh37.p13 chr19: 1,021,959-1,037,277 RNU6-2, CNN2
    nsv5518287copy number variation1nstd206human GRCh38 chr19: 1,020,171-1,020,311 , GRCh37.p13 chr19: 1,020,170-1,020,310 RNU6-2, TMEM259
    nsv5328740copy number variation1nstd204human GRCh38.p13 chr19: 928,886-1,307,166 , GRCh37.p13 chr19: 928,886-1,307,165 RNU6-2, CNN2, 25 more genes
    nsv5327588copy number variation1nstd204human GRCh38.p13 chr19: 502,284-1,164,314 , GRCh37.p13 chr19: 502,284-1,164,313 RPS2P52, PRSS57, 44 more genes
    nsv5298972copy number variation1nstd204human GRCh38.p13 chr19: 1,009,162-1,020,673 , GRCh37.p13 chr19: 1,009,161-1,020,672 RNU6-2, GRIN3B, 1 more genes
    nsv5291406copy number variation1nstd204human GRCh38.p13 chr19: 1,016,701-1,035,100 , GRCh37.p13 chr19: 1,016,700-1,035,099 RNU6-2, CNN2, 1 more genes
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
    nsv5286922copy number variation1nstd204human GRCh38.p13 chr19: 928,601-1,137,200 , GRCh37.p13 chr19: 928,601-1,137,199 POLR2E, SBNO2, 10 more genes
    nsv5285488copy number variation1nstd204human GRCh37.p13 chr19: 1,007,082-1,049,604 , GRCh38.p13 chr19: 1,007,083-1,049,605 CNN2, ABCA7, 4 more genes
    nsv5283439copy number variation1nstd204human GRCh38.p13 chr19: 879,901-1,335,800 , GRCh37.p13 chr19: 879,901-1,335,799 ATP5F1D, LOC107985303, 29 more genes
    nsv5282241copy number variation1nstd204human GRCh38.p13 chr19: 1,016,224-1,032,467 , GRCh37.p13 chr19: 1,016,223-1,032,466 RNU6-2, CNN2, 1 more genes
    nsv5029164copy number variation1nstd200human GRCh38 chr19: 502,290-1,164,305 , GRCh37.p13 chr19: 502,290-1,164,304 LOC105372235, RNU6-2, 44 more genes
    nsv5019009copy number variation1nstd200human GRCh38 chr19: 1,020,171-1,020,311 , GRCh37.p13 chr19: 1,020,170-1,020,310 TMEM259, RNU6-2
    nsv4854880copy number variation1nstd200human GRCh37 chr19: 928,895-1,307,157 , GRCh38.p12 chr19: 928,895-1,307,158 CIRBP, ABCA7, 25 more genes
    nsv4854867copy number variation1nstd200human GRCh37 chr19: 502,290-1,164,304 , GRCh38.p12 chr19: 502,290-1,164,305 LOC100420586, BSG, 44 more genes
    nsv4683365copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,926-1,401,495 , GRCh38.p12 chr19: 589,926-1,401,496 MISP, STK11, 56 more genes
    nsv4681084copy number variation1nstd102humanPathogenic GRCh37 chr19: 852,326-1,226,646 , GRCh38.p12 chr19: 852,326-1,226,647 CBARP, RNU6-9, 21 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4631882copy number variation1nstd183human GRCh37 chr19: 970,774-1,135,485 , GRCh38.p12 chr19: 970,774-1,135,486 RNU6-2, LOC105372235, 10 more genes
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