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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939049copy number variation1nstd209human GRCh38 chr19: 10,464,317-10,465,438 , GRCh37.p13 chr19: 10,574,993-10,576,114 PDE4A
    nsv5886302copy number variation1nstd209human GRCh38 chr19: 10,464,254-10,465,303 , GRCh37.p13 chr19: 10,574,930-10,575,979 PDE4A
    nsv5523949copy number variation1nstd206human GRCh38 chr19: 10,425,964-10,426,795 , GRCh37.p13 chr19: 10,536,640-10,537,471 PDE4A
    nsv5521725copy number variation1nstd206human GRCh38 chr19: 10,464,060-10,464,343 , GRCh37.p13 chr19: 10,574,736-10,575,019 PDE4A
    nsv5515582copy number variation1nstd206human GRCh38 chr19: 10,436,469-10,436,523 , GRCh37.p13 chr19: 10,547,145-10,547,199 PDE4A
    nsv5375304translocation1nstd200human GRCh38 chr19: 10,475,017-10,475,017 , GRCh38 chr19: 10,469,974-10,469,974 , GRCh37.p13 chr19: 10,585,693-10,585,693 , GRCh37.p13 chr19: 10,580,650-10,580,650 PDE4A
    nsv5359461translocation1nstd200human GRCh38 chr19: 9,181,072-9,181,072 , GRCh38 chr19: 10,460,428-10,460,428 , GRCh37.p13 chr19: 9,291,748-9,291,748 , GRCh37.p13 chr19: 10,571,104-10,571,104 PDE4A, ELOCP29
    nsv5344080translocation1nstd200human GRCh37 chr19: 10,580,650-10,580,650 , GRCh37 chr19: 10,585,693-10,585,693 , GRCh38.p12 chr19: 10,475,017-10,475,017 , GRCh38.p12 chr19: 10,469,974-10,469,974 PDE4A
    nsv5321786copy number variation1nstd204human GRCh38.p13 chr19: 10,464,057-10,464,344 , GRCh37.p13 chr19: 10,574,733-10,575,020 PDE4A
    nsv5321619copy number variation1nstd204human GRCh38.p13 chr19: 10,406,948-10,466,345 , GRCh37.p13 chr19: 10,517,624-10,577,021 PDE4A
    nsv5292687copy number variation1nstd204human GRCh38.p13 chr19: 10,416,931-10,420,146 , GRCh37.p13 chr19: 10,527,607-10,530,822 PDE4A
    nsv5291380copy number variation1nstd204human GRCh38.p13 chr19: 10,335,201-10,670,200 , GRCh37.p13 chr19: 10,445,877-10,780,876 ICAM3, MIR1181, 15 more genes
    nsv5288335copy number variation1nstd204human GRCh38.p13 chr19: 10,435,895-10,438,069 , GRCh37.p13 chr19: 10,546,571-10,548,745 PDE4A
    nsv5287671copy number variation1nstd204human GRCh38.p13 chr19: 10,406,701-10,466,300 , GRCh37.p13 chr19: 10,517,377-10,576,976 PDE4A
    nsv5287567copy number variation1nstd204human GRCh38.p13 chr19: 10,406,765-10,460,761 , GRCh37.p13 chr19: 10,517,441-10,571,437 PDE4A
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5284133copy number variation1nstd204human GRCh38.p13 chr19: 10,433,601-10,448,300 , GRCh37.p13 chr19: 10,544,277-10,558,976 PDE4A
    nsv5165995mobile element insertion1nstd203human GRCh38 chr19: 10,441,845-10,441,869 , GRCh37.p13 chr19: 10,552,521-10,552,545 PDE4A
    nsv5014509copy number variation1nstd200human GRCh38 chr19: 10,465,399-10,477,114 , GRCh37.p13 chr19: 10,576,075-10,587,790 PDE4A
    nsv5014508copy number variation1nstd200human GRCh38 chr19: 10,448,073-10,449,540 , GRCh37.p13 chr19: 10,558,749-10,560,216 PDE4A
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