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Items: 1 to 20 of 752

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980095insertion1nstd209human GRCh38 chr14: 35,172,453-35,172,453 , GRCh37.p13 chr14: 35,641,659-35,641,659 PRORP
    nsv5974708insertion1nstd209human GRCh38 chr14: 35,216,103-35,216,103 , GRCh37.p13 chr14: 35,685,309-35,685,309 PRORP
    nsv5942595copy number variation1nstd209human GRCh38 chr14: 35,151,848-35,152,005 , GRCh37.p13 chr14: 35,621,054-35,621,211 PRORP
    nsv5940194copy number variation1nstd209human GRCh38 chr14: 35,136,408-35,145,861 , GRCh37.p13 chr14: 35,605,614-35,615,067 RPL23AP70, PRORP
    nsv5936396copy number variation1nstd209human GRCh38 chr14: 35,233,086-35,233,671 , GRCh37.p13 chr14: 35,702,292-35,702,877 RPL7AP3, PRORP
    nsv5930047copy number variation1nstd209human GRCh38 chr14: 35,042,551-35,131,102 , GRCh37.p13 chr14: 35,511,757-35,600,308 PRORP, PPP2R3C, 2 more genes
    nsv5864083copy number variation1nstd209human GRCh38 chr14: 35,136,447-35,143,126 , GRCh37.p13 chr14: 35,605,653-35,612,332 PRORP, RPL23AP70
    nsv5859842copy number variation1nstd209human GRCh38 chr14: 35,129,747-35,130,946 , GRCh37.p13 chr14: 35,598,953-35,600,152 PRORP
    nsv5730116mobile element insertion2nstd211human GRCh38 chr14: 35,230,070-35,230,070 , GRCh37.p13 chr14: 35,699,276-35,699,276 PRORP
    nsv5710892mobile element insertion1nstd211human GRCh38 chr14: 35,172,468-35,172,468 , GRCh37.p13 chr14: 35,641,674-35,641,674 PRORP
    nsv5709554mobile element insertion1nstd211human GRCh38 chr14: 35,243,650-35,243,650 , GRCh37.p13 chr14: 35,712,856-35,712,856 PRORP
    nsv5696691mobile element insertion1nstd211human GRCh38 chr14: 35,240,313-35,240,313 , GRCh37.p13 chr14: 35,709,519-35,709,519 PRORP
    nsv5664454insertion1nstd207human GRCh38 chr14: 35,172,453-35,172,453 , GRCh37.p13 chr14: 35,641,659-35,641,659 PRORP
    nsv5655686insertion1nstd207human GRCh38 chr14: 35,216,103-35,216,103 , GRCh37.p13 chr14: 35,685,309-35,685,309 PRORP
    nsv5599458copy number variation1nstd207human GRCh38 chr14: 35,136,408-35,145,861 , GRCh37.p13 chr14: 35,605,614-35,615,067 RPL23AP70, PRORP
    nsv5593401copy number variation1nstd207human GRCh38 chr14: 35,233,086-35,233,671 , GRCh37.p13 chr14: 35,702,292-35,702,877 RPL7AP3, PRORP
    nsv5513073copy number variation1nstd206human GRCh38 chr14: 35,227,375-35,250,189 , GRCh37.p13 chr14: 35,696,581-35,719,395 RPL7AP3, PRORP
    nsv5511997copy number variation1nstd206human GRCh38 chr14: 35,120,018-35,120,445 , GRCh37.p13 chr14: 35,589,224-35,589,651 PRORP, PPP2R3C
    nsv5505373copy number variation1nstd206human GRCh38 chr14: 35,140,379-35,140,430 , GRCh37.p13 chr14: 35,609,585-35,609,636 PRORP
    nsv5501529copy number variation1nstd206human GRCh38 chr14: 35,233,089-35,233,672 , GRCh37.p13 chr14: 35,702,295-35,702,878 PRORP, RPL7AP3
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