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Items: 1 to 20 of 351

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924462copy number variation1nstd209human GRCh38 chr8: 30,619,496-30,625,633 , GRCh37.p13 chr8: 30,477,013-30,483,150 GTF2E2
    nsv5918470copy number variation1nstd209human GRCh38 chr8: 30,652,975-30,653,097 , GRCh37.p13 chr8: 30,510,492-30,510,614 GTF2E2
    nsv5910343copy number variation1nstd209human GRCh38 chr8: 30,614,907-30,623,971 , GRCh37.p13 chr8: 30,472,424-30,481,488 GTF2E2
    nsv5853965copy number variation1nstd209human GRCh38 chr8: 30,622,716-30,625,659 , GRCh37.p13 chr8: 30,480,233-30,483,176 GTF2E2
    nsv5853384copy number variation1nstd209human GRCh38 chr8: 30,618,870-30,624,251 , GRCh37.p13 chr8: 30,476,387-30,481,768 GTF2E2
    nsv5852661copy number variation1nstd209human GRCh38 chr8: 30,614,870-30,621,215 , GRCh37.p13 chr8: 30,472,387-30,478,732 GTF2E2
    nsv5633108insertion1nstd207human GRCh38 chr8: 30,583,976-30,583,976 , GRCh37.p13 chr8: 30,441,493-30,441,493 GTF2E2
    nsv5549678insertion1nstd206human GRCh38 chr8: 30,583,987-30,584,022 , GRCh37.p13 chr8: 30,441,504-30,441,539 GTF2E2
    nsv5491995copy number variation1nstd206human GRCh38 chr8: 30,619,496-30,625,634 , GRCh37.p13 chr8: 30,477,013-30,483,151 GTF2E2
    nsv5486328copy number variation1nstd206human GRCh38 chr8: 30,614,909-30,623,972 , GRCh37.p13 chr8: 30,472,426-30,481,489 GTF2E2
    nsv5484960copy number variation1nstd206human GRCh38 chr8: 30,590,979-30,593,737 , GRCh37.p13 chr8: 30,448,496-30,451,254 GTF2E2
    nsv5363978translocation1nstd200human GRCh38 chr8: 30,631,108-30,631,108 , GRCh38 chr8: 30,631,050-30,631,050 , GRCh37.p13 chr8: 30,488,625-30,488,625 , GRCh37.p13 chr8: 30,488,567-30,488,567 GTF2E2
    nsv5363977translocation1nstd200human GRCh38 chr8: 30,614,909-30,614,909 , GRCh38 chr8: 30,623,972-30,623,972 , GRCh37.p13 chr8: 30,472,426-30,472,426 , GRCh37.p13 chr8: 30,481,489-30,481,489 GTF2E2
    nsv5344582translocation1nstd200human GRCh37 chr8: 30,547,968-30,547,968 , GRCh37 chr8: 30,438,466-30,438,466 , GRCh38.p12 chr8: 30,580,949-30,580,949 , GRCh38.p12 chr8: 30,690,451-30,690,451 GTF2E2, GSR
    nsv5312462copy number variation1nstd204human GRCh38.p13 chr8: 30,619,491-30,625,643 , GRCh37.p13 chr8: 30,477,008-30,483,160 GTF2E2
    nsv5301473copy number variation1nstd204human GRCh38.p13 chr8: 30,572,869-30,699,580 , GRCh37.p13 chr8: 30,430,386-30,557,097 , RNU5A-3P, 3 more genes
    nsv5260011copy number variation1nstd204human GRCh38.p13 chr8: 30,631,960-30,634,959 , GRCh37.p13 chr8: 30,489,477-30,492,476 GTF2E2
    nsv5259213copy number variation1nstd204human GRCh38.p13 chr8: 30,570,768-30,604,887 , GRCh37.p13 chr8: 30,428,285-30,462,404 , GTF2E2, 1 more genes
    nsv5259100copy number variation1nstd204human GRCh38.p13 chr8: 30,619,470-30,625,822 , GRCh37.p13 chr8: 30,476,987-30,483,339 GTF2E2
    nsv5259027copy number variation1nstd204human GRCh38.p13 chr8: 30,592,701-30,596,400 , GRCh37.p13 chr8: 30,450,218-30,453,917 GTF2E2
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