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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131202insertion1nstd186human GRCh37 chr19: 54,402,184-54,402,187 , GRCh38.p12 chr19: 53,898,930-53,898,933 PRKCG
    nsv5970445insertion1nstd209human GRCh38 chr19: 53,898,914-53,898,914 , GRCh37.p13 chr19: 54,402,168-54,402,168 PRKCG
    nsv5945695copy number variation1nstd209human GRCh38 chr19: 53,880,682-53,880,733 , GRCh37.p13 chr19: 54,383,936-54,383,987 PRKCG
    nsv5941082copy number variation1nstd209human GRCh38 chr19: 53,880,249-53,880,456 , GRCh37.p13 chr19: 54,383,503-54,383,710 PRKCG
    nsv5935137copy number variation1nstd209human GRCh38 chr19: 52,932,265-54,037,356 , GRCh37.p13 chr19: 53,435,518-54,528,887 LOC107987264, CACNG6, 113 more genes
    nsv5933123copy number variation1nstd209human GRCh38 chr19: 53,880,554-53,880,807 , GRCh37.p13 chr19: 54,383,808-54,384,061 PRKCG
    nsv5931037copy number variation1nstd209human GRCh38 chr19: 53,760,924-54,051,285 , GRCh37.p13 chr19: 54,264,178-54,528,887 CACNG6, HMGN1P32, 17 more genes
    nsv5661349insertion1nstd207human GRCh38 chr19: 53,906,120-53,906,120 , GRCh37.p13 chr19: 54,409,374-54,409,374 PRKCG
    nsv5649317insertion1nstd207human GRCh38 chr19: 53,898,914-53,898,914 , GRCh37.p13 chr19: 54,402,168-54,402,168 PRKCG
    nsv5601405copy number variation1nstd207human GRCh38 chr19: 53,880,312-53,880,423 , GRCh37.p13 chr19: 54,383,566-54,383,677 PRKCG
    nsv5598205copy number variation1nstd207human GRCh38 chr19: 53,906,054-53,906,104 , GRCh37.p13 chr19: 54,409,308-54,409,358 PRKCG
    nsv5564521insertion1nstd102humanUncertain significance GRCh38 chr19: 53,880,584-53,880,584 , GRCh37 chr19: 54,383,838-54,383,838 PRKCG
    nsv5550263insertion1nstd206human GRCh38 chr19: 53,898,930-53,898,933 , GRCh37.p13 chr19: 54,402,184-54,402,187 PRKCG
    nsv5522128copy number variation1nstd206human GRCh38 chr19: 53,880,983-53,881,146 , GRCh37.p13 chr19: 54,384,237-54,384,400 PRKCG
    nsv5520318copy number variation1nstd206human GRCh38 chr19: 53,890,404-53,890,938 , GRCh37.p13 chr19: 54,393,658-54,394,192 PRKCG
    nsv5393404copy number variation1nstd186human GRCh37 chr19: 54,383,483-54,383,683 , GRCh38.p12 chr19: 53,880,229-53,880,429 PRKCG
    nsv5391446copy number variation1nstd186human GRCh37 chr19: 54,383,411-54,383,838 , GRCh38.p12 chr19: 53,880,157-53,880,584 PRKCG
    nsv5381201copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,297,303-54,410,149 , GRCh38.p12 chr19: 53,794,049-53,906,895 MYADM-AS1, MYADM, 2 more genes
    nsv5328960copy number variation1nstd204human GRCh38.p13 chr19: 53,880,021-53,880,525 , GRCh37.p13 chr19: 54,383,275-54,383,779 PRKCG
    nsv5021299copy number variation1nstd200human GRCh38 chr19: 53,880,157-53,880,584 , GRCh37.p13 chr19: 54,383,411-54,383,838 PRKCG
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