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Items: 1 to 20 of 45

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672818copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,590,523-95,599,795 , GRCh38.p12 chr14: 95,124,186-95,133,458 DICER1
    nsv4769268copy number variation1nstd102humanPathogenic GRCh38 chr14: 95,108,718-95,115,707 , GRCh37 chr14: 95,575,055-95,582,044 DICER1
    nsv4685665copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,559,191-95,563,091 , GRCh38 chr14: 95,092,854-95,096,754 DICER1
    nsv3879786copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,559,869-95,560,991 , GRCh38 chr14: 95,093,532-95,094,654 DICER1
    nsv5672577copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,578,499-95,579,571 , GRCh38.p12 chr14: 95,112,162-95,113,234 DICER1
    nsv4450231copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr14: 95,556,825-95,599,805 , GRCh38 chr14: 95,090,488-95,133,468 DICER1
    nsv4682344copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr14: 95,556,835-95,599,795 , GRCh38.p12 chr14: 95,090,498-95,133,458 DICER1
    nsv4685789delins1nstd102humanPathogenic GRCh37 chr14: 95,567,552-95,570,469 , GRCh38 chr14: 95,101,215-95,104,132 DICER1
    nsv7094274copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 95,568,083-95,569,716 , GRCh38.p12 chr14: 95,101,746-95,103,379 DICER1
    nsv7137052copy number variation1nstd102humanUncertain significance GRCh37 chr14: 95,573,300-95,579,699 , GRCh38 chr14: 95,106,963-95,113,362 DICER1
    nsv3877287copy number variation1nstd102humanUncertain significance GRCh37 chr14: 95,552,565-95,599,840 , GRCh38 chr14: 95,086,228-95,133,503 DICER1
    nsv3877218copy number variation1nstd102humanUncertain significance GRCh38 chr14: 95,111,307-95,133,468 , GRCh37 chr14: 95,577,644-95,599,805 DICER1
    nsv6309770copy number variation1nstd102humanUncertain significance GRCh37 chr14: 95,577,644-95,599,795 , GRCh38.p12 chr14: 95,111,307-95,133,458 DICER1
    nsv4453657copy number variation1nstd102humanUncertain significance GRCh38 chr14: 95,090,488-95,096,723 , GRCh37 chr14: 95,556,825-95,563,060 DICER1
    nsv7094273copy number variation1nstd102humanUncertain significance GRCh37 chr14: 95,556,835-95,563,060 , GRCh38.p12 chr14: 95,090,498-95,096,723 DICER1
    nsv3170323copy number variation1nstd45humanPathogenic GRCh38.p12 chr14: 95,086,228-95,158,010 , GRCh37 chr14: 95,552,565-95,624,347 DICER1, DICER1-AS1, 1 more genes
    nsv4729371copy number variation1nstd102humanUncertain significance GRCh37 chr14: 95,465,399-95,752,464 , GRCh38.p12 chr14: 94,999,062-95,286,127 DICER1, MIR3173, 2 more genes
    nsv4681745copy number variation1nstd102humanUncertain significance GRCh37 chr14: 95,551,565-95,624,759 , GRCh38.p12 chr14: 95,085,228-95,158,422 DICER1, DICER1-AS1, 1 more genes
    nsv3893892copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,137-96,908,198 , GRCh38.p12 chr14: 84,316,793-96,441,861 DICER1, SERPINA13P, 175 more genes
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 DICER1, SHLD2P2, 175 more genes
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