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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939150copy number variation1nstd209human GRCh38 chr19: 1,092,422-1,092,905 , GRCh37.p13 chr19: 1,092,421-1,092,904 POLR2E
    nsv5929610copy number variation1nstd209human GRCh38 chr19: 1,085,483-1,085,584 , GRCh37.p13 chr19: 1,085,482-1,085,583 POLR2E, ARHGAP45
    nsv5648949insertion1nstd207human GRCh38 chr19: 1,092,667-1,092,667 , GRCh37.p13 chr19: 1,092,666-1,092,666 POLR2E
    nsv5532495copy number variation1nstd206human GRCh38 chr19: 1,085,478-1,085,605 , GRCh37.p13 chr19: 1,085,477-1,085,604 POLR2E, ARHGAP45
    nsv5520404copy number variation1nstd206human GRCh38 chr19: 1,092,417-1,092,955 , GRCh37.p13 chr19: 1,092,416-1,092,954 POLR2E
    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
    nsv5324086copy number variation1nstd204human GRCh38.p13 chr19: 1,093,165-1,094,502 , GRCh37.p13 chr19: 1,093,164-1,094,501 POLR2E
    nsv5299117copy number variation1nstd204human GRCh37.p13 chr19: 1,035,100-1,137,199 , GRCh38.p13 chr19: 1,035,101-1,137,200 CNN2, GPX4, 4 more genes
    nsv5298409copy number variation1nstd204human GRCh38.p13 chr19: 1,083,911-1,087,461 , GRCh37.p13 chr19: 1,083,910-1,087,460 POLR2E, ARHGAP45
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
    nsv5290929copy number variation1nstd204human GRCh38.p13 chr19: 1,080,303-1,125,403 , GRCh37.p13 chr19: 1,080,302-1,125,402 SBNO2, ARHGAP45, 2 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
    nsv5283439copy number variation1nstd204human GRCh38.p13 chr19: 879,901-1,335,800 , GRCh37.p13 chr19: 879,901-1,335,799 ATP5F1D, LOC107985303, 29 more genes
    nsv5196747mobile element insertion1nstd203human GRCh38 chr19: 1,085,238-1,085,256 , GRCh37.p13 chr19: 1,085,237-1,085,255 POLR2E, ARHGAP45
    nsv5029164copy number variation1nstd200human GRCh38 chr19: 502,290-1,164,305 , GRCh37.p13 chr19: 502,290-1,164,304 LOC105372235, RNU6-2, 44 more genes
    nsv5019015copy number variation1nstd200human GRCh38 chr19: 1,093,170-1,094,496 , GRCh37.p13 chr19: 1,093,169-1,094,495 POLR2E
    nsv4868080copy number variation1nstd200human GRCh37 chr19: 1,093,169-1,094,495 , GRCh38.p12 chr19: 1,093,170-1,094,496 POLR2E
    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
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