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Items: 1 to 20 of 491

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926753copy number variation1nstd209human GRCh38 chr10: 35,017,338-35,017,398 , GRCh37.p13 chr10: 35,306,266-35,306,326 CUL2
    nsv5926262copy number variation1nstd209human GRCh38 chr10: 34,690,970-35,012,521 , GRCh37.p13 chr10: 34,979,898-35,301,449 CUL2, PARD3, 6 more genes
    nsv5917198copy number variation1nstd209human GRCh38 chr10: 35,065,278-35,065,357 , GRCh37.p13 chr10: 35,354,206-35,354,285 CUL2
    nsv5916272copy number variation1nstd209human GRCh38 chr10: 34,890,792-35,036,875 , GRCh37.p13 chr10: 35,179,720-35,325,803 RNU6-847P, CUL2, 3 more genes
    nsv5915715copy number variation1nstd209human GRCh38 chr10: 35,038,656-35,038,732 , GRCh37.p13 chr10: 35,327,584-35,327,660 CUL2
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5911333copy number variation1nstd209human GRCh38 chr10: 35,042,122-35,043,385 , GRCh37.p13 chr10: 35,331,050-35,332,313 CUL2
    nsv5907671copy number variation1nstd209human GRCh38 chr10: 35,076,064-35,077,201 , GRCh37.p13 chr10: 35,364,992-35,366,129 CUL2
    nsv5866101copy number variation1nstd209human GRCh38 chr10: 35,009,269-35,041,575 , GRCh37.p13 chr10: 35,298,197-35,330,503 CUL2
    nsv5862005copy number variation2nstd209human GRCh38 chr10: 35,075,952-35,077,002 , GRCh37.p13 chr10: 35,364,880-35,365,930 CUL2
    nsv5860517copy number variation1nstd209human GRCh38 chr10: 35,030,438-35,050,781 , GRCh37.p13 chr10: 35,319,366-35,339,709 CUL2
    nsv5857766copy number variation2nstd209human GRCh38 chr10: 35,042,176-35,043,375 , GRCh37.p13 chr10: 35,331,104-35,332,303 CUL2
    nsv5724131mobile element insertion2nstd211human GRCh38 chr10: 35,049,936-35,049,936 , GRCh37.p13 chr10: 35,338,864-35,338,864 CUL2
    nsv5632354insertion1nstd207human GRCh38 chr10: 35,049,922-35,049,922 , GRCh37.p13 chr10: 35,338,850-35,338,850 CUL2
    nsv5589317copy number variation1nstd207human GRCh38 chr10: 35,042,122-35,043,385 , GRCh37.p13 chr10: 35,331,050-35,332,313 CUL2
    nsv5560407mobile element insertion1nstd206human GRCh38 chr10: 35,049,936-35,049,987 , GRCh37.p13 chr10: 35,338,864-35,338,915 CUL2
    nsv5549346insertion1nstd206human GRCh38 chr10: 35,120,924-35,120,959 , GRCh37.p13 chr10: 35,409,852-35,409,887 CUL2
    nsv5488475copy number variation1nstd206human GRCh38 chr10: 35,040,975-35,041,045 , GRCh37.p13 chr10: 35,329,903-35,329,973 CUL2
    nsv5487429copy number variation1nstd206human GRCh38 chr10: 35,042,124-35,043,386 , GRCh37.p13 chr10: 35,331,052-35,332,314 CUL2
    nsv5484233copy number variation1nstd206human GRCh38 chr10: 35,018,244-35,023,000 , GRCh37.p13 chr10: 35,307,172-35,311,928 CUL2
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