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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960053insertion1nstd209human GRCh38 chr5: 150,656,741-150,656,741 , GRCh37.p13 chr5: 150,036,303-150,036,303 SYNPO
    nsv5889133copy number variation1nstd209human GRCh38 chr5: 150,588,392-150,594,076 , GRCh37.p13 chr5: 149,967,954-149,973,638 SYNPO
    nsv5841489copy number variation1nstd209human GRCh38 chr5: 150,588,361-150,594,035 , GRCh37.p13 chr5: 149,967,923-149,973,597 SYNPO
    nsv5693062mobile element insertion1nstd211human GRCh38 chr5: 150,597,194-150,597,194 , GRCh37.p13 chr5: 149,976,756-149,976,756 SYNPO
    nsv5473469copy number variation1nstd206human GRCh38 chr5: 150,641,051-150,644,591 , GRCh37.p13 chr5: 150,020,613-150,024,153 SYNPO
    nsv5472676copy number variation1nstd206human GRCh38 chr5: 150,626,818-150,626,871 , GRCh37.p13 chr5: 150,006,380-150,006,433 SYNPO
    nsv5464934copy number variation1nstd206human GRCh38 chr5: 150,657,670-150,657,754 , GRCh37.p13 chr5: 150,037,232-150,037,316 SYNPO
    nsv5461461copy number variation1nstd206human GRCh38 chr5: 150,652,608-150,670,289 , GRCh37.p13 chr5: 150,032,170-150,049,851 MYOZ3, SYNPO
    nsv5461355copy number variation1nstd206human GRCh38 chr5: 150,622,711-150,622,801 , GRCh37.p13 chr5: 150,002,273-150,002,363 SYNPO
    nsv5456499copy number variation1nstd206human GRCh38 chr5: 150,599,006-150,599,113 , GRCh37.p13 chr5: 149,978,568-149,978,675 SYNPO
    nsv5456286copy number variation1nstd206human GRCh38 chr5: 150,652,701-150,652,758 , GRCh37.p13 chr5: 150,032,263-150,032,320 SYNPO
    nsv5406629mobile element insertion1nstd206human GRCh38 chr5: 150,597,194-150,597,245 , GRCh37.p13 chr5: 149,976,756-149,976,807 SYNPO
    nsv5362539translocation1nstd200human GRCh38 chr5: 150,652,758-150,652,758 , GRCh38 chr5: 150,652,701-150,652,701 , GRCh37.p13 chr5: 150,032,263-150,032,263 , GRCh37.p13 chr5: 150,032,320-150,032,320 SYNPO
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4939182copy number variation1nstd200human GRCh38 chr5: 150,587,551-150,588,488 , GRCh37.p13 chr5: 149,967,113-149,968,050 SYNPO
    nsv4939180copy number variation1nstd200human GRCh38 chr5: 150,574,626-150,584,462 , GRCh37.p13 chr5: 149,954,188-149,964,024 SYNPO
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4814968copy number variation1nstd200human GRCh37 chr5: 149,967,113-149,968,050 , GRCh38.p12 chr5: 150,587,551-150,588,488 SYNPO
    nsv4814967copy number variation1nstd200human GRCh37 chr5: 149,954,188-149,964,024 , GRCh38.p12 chr5: 150,574,626-150,584,462 SYNPO
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