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Items: 1 to 20 of 441

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960286insertion1nstd209human GRCh38 chr8: 27,438,462-27,438,462 , GRCh37.p13 chr8: 27,295,979-27,295,979 PTK2B
    nsv5959095insertion1nstd209human GRCh38 chr8: 27,350,991-27,350,991 , GRCh37.p13 chr8: 27,208,508-27,208,508 PTK2B
    nsv5926482copy number variation1nstd209human GRCh38 chr8: 27,369,638-27,369,944 , GRCh37.p13 chr8: 27,227,155-27,227,461 PTK2B
    nsv5924408copy number variation1nstd209human GRCh38 chr8: 27,322,795-27,322,883 , GRCh37.p13 chr8: 27,180,312-27,180,400 PTK2B
    nsv5919019copy number variation1nstd209human GRCh38 chr8: 26,939,516-27,553,947 , GRCh37.p13 chr8: 26,797,033-27,411,464 LOC105379339, TRIM35, 9 more genes
    nsv5717987mobile element insertion2nstd211human GRCh38 chr8: 27,350,979-27,350,979 , GRCh37.p13 chr8: 27,208,496-27,208,496 PTK2B
    nsv5712878mobile element insertion1nstd211human GRCh38 chr8: 27,369,182-27,369,182 , GRCh37.p13 chr8: 27,226,699-27,226,699 PTK2B
    nsv5704544mobile element insertion1nstd211human GRCh38 chr8: 27,441,442-27,441,442 , GRCh37.p13 chr8: 27,298,959-27,298,959 PTK2B
    nsv5702301mobile element insertion2nstd211human GRCh38 chr8: 27,350,991-27,350,991 , GRCh37.p13 chr8: 27,208,508-27,208,508 PTK2B
    nsv5696433mobile element insertion1nstd211human GRCh38 chr8: 27,338,213-27,338,213 , GRCh37.p13 chr8: 27,195,730-27,195,730 PTK2B
    nsv5637029insertion1nstd207human GRCh38 chr8: 27,438,462-27,438,462 , GRCh37.p13 chr8: 27,295,979-27,295,979 PTK2B
    nsv5579418copy number variation1nstd207human GRCh38 chr8: 27,322,795-27,322,883 , GRCh37.p13 chr8: 27,180,312-27,180,400 PTK2B
    nsv5545891insertion1nstd206human GRCh38 chr8: 27,438,462-27,438,462 , GRCh37.p13 chr8: 27,295,979-27,295,979 PTK2B
    nsv5490612copy number variation1nstd206human GRCh38 chr8: 27,393,438-27,393,496 , GRCh37.p13 chr8: 27,250,955-27,251,013 PTK2B
    nsv5489658copy number variation1nstd206human GRCh38 chr8: 27,406,450-27,408,862 , GRCh37.p13 chr8: 27,263,967-27,266,379 PTK2B
    nsv5489241copy number variation1nstd206human GRCh38 chr8: 27,275,976-27,445,064 , GRCh37.p13 chr8: 27,133,493-27,302,581 PTK2B, TRIM35, 1 more genes
    nsv5487287copy number variation1nstd206human GRCh38 chr8: 27,303,949-27,359,404 , GRCh37.p13 chr8: 27,161,466-27,216,921 PTK2B, TRIM35
    nsv5484487copy number variation1nstd206human GRCh38 chr8: 27,322,796-27,322,884 , GRCh37.p13 chr8: 27,180,313-27,180,401 PTK2B
    nsv5481253copy number variation1nstd206human GRCh38 chr8: 27,402,172-27,405,342 , GRCh37.p13 chr8: 27,259,689-27,262,859 PTK2B
    nsv5479406copy number variation1nstd206human GRCh38 chr8: 27,402,345-27,408,345 , GRCh37.p13 chr8: 27,259,862-27,265,862 PTK2B
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