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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5943830copy number variation1nstd209human GRCh38 chr19: 18,261,533-18,261,766 , GRCh37.p13 chr19: 18,372,343-18,372,576 IQCN
    nsv5942188copy number variation1nstd209human GRCh38 chr19: 18,260,807-18,261,238 , GRCh37.p13 chr19: 18,371,617-18,372,048 IQCN
    nsv5939481copy number variation1nstd209human GRCh38 chr19: 18,273,310-18,273,609 , GRCh37.p13 chr19: 18,384,120-18,384,419 IQCN
    nsv5929458copy number variation1nstd209human GRCh38 chr19: 18,261,539-18,261,967 , GRCh37.p13 chr19: 18,372,349-18,372,777 IQCN
    nsv5531963copy number variation1nstd206human GRCh38 chr19: 18,251,668-18,256,033 , GRCh37.p13 chr19: 18,362,478-18,366,843 CIST1, IQCN
    nsv5299651copy number variation1nstd204human GRCh38.p13 chr19: 16,996,101-18,292,600 , GRCh37.p13 chr19: 17,106,911-18,403,410 ANO8, MPV17L2, 57 more genes
    nsv5284071copy number variation1nstd204human GRCh38.p13 chr19: 17,954,901-18,442,000 , GRCh37.p13 chr19: 18,065,710-18,552,810 ISYNA1, LOC105372300, 27 more genes
    nsv5164884mobile element insertion1nstd203human GRCh38 chr19: 18,272,379-18,272,425 , GRCh37.p13 chr19: 18,383,189-18,383,235 IQCN
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4860621copy number variation1nstd200human GRCh37 chr19: 18,382,907-18,383,694 , GRCh38.p12 chr19: 18,272,097-18,272,884 IQCN
    nsv4860620copy number variation1nstd200human GRCh37 chr19: 18,371,721-18,372,177 , GRCh38.p12 chr19: 18,260,911-18,261,367 IQCN
    nsv4860619copy number variation1nstd200human GRCh37 chr19: 18,371,607-18,372,017 , GRCh38.p12 chr19: 18,260,797-18,261,207 IQCN
    nsv4769776mobile element deletion1nstd200human GRCh37 chr19: 18,383,426-18,383,720 , GRCh38.p12 chr19: 18,272,616-18,272,910 IQCN
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4533646copy number variation1nstd166human GRCh37.p13 chr19: 18,382,866-18,383,671 , GRCh38.p12 chr19: 18,272,056-18,272,861 IQCN
    nsv4382739copy number variation1nstd173human GRCh37 chr19: 18,367,755-18,399,375 , GRCh38.p12 chr19: 18,256,945-18,288,565 RPL39P38, JUND, 2 more genes
    nsv4271919copy number variation1nstd166human GRCh37.p13 chr19: 18,371,626-18,372,017 , GRCh38.p12 chr19: 18,260,816-18,261,207 IQCN
    nsv4266019copy number variation1nstd166human GRCh37.p13 chr19: 18,375,932-18,376,008 , GRCh38.p12 chr19: 18,265,122-18,265,198 IQCN
    nsv4255882copy number variation1nstd166human GRCh37.p13 chr19: 18,371,071-18,373,885 , GRCh38.p12 chr19: 18,260,261-18,263,075 IQCN
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