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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954386copy number variation1nstd209human GRCh38 chr20: 23,624,854-23,624,925 , GRCh37.p13 chr20: 23,605,491-23,605,562 CST3
    nsv5599840copy number variation1nstd207human GRCh38 chr20: 23,624,850-23,624,925 , GRCh37.p13 chr20: 23,605,487-23,605,562 CST3
    nsv5021768copy number variation1nstd200human GRCh38 chr20: 23,625,717-23,627,685 , GRCh37.p13 chr20: 23,606,354-23,608,322 CST3
    nsv4738033copy number variation1nstd199human GRCh37 chr20: 23,605,449-23,605,517 , GRCh38.p12 chr20: 23,624,812-23,624,880 CST3
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4667366copy number variation1nstd186human GRCh37 chr20: 23,618,325-23,619,120 , GRCh38.p12 chr20: 23,637,688-23,638,483 CST3
    nsv4633051copy number variation1nstd183human GRCh37 chr20: 23,619,073-23,622,427 , GRCh38.p12 chr20: 23,638,436-23,641,790 CST3
    nsv4632749copy number variation1nstd183human GRCh37 chr20: 23,618,522-23,622,427 , GRCh38.p12 chr20: 23,637,885-23,641,790 CST3
    nsv4624082copy number variation1nstd183human GRCh37 chr20: 23,619,063-23,619,121 , GRCh38.p12 chr20: 23,638,426-23,638,484 CST3
    nsv4623279copy number variation1nstd183human GRCh37 chr20: 23,618,325-23,619,120 , GRCh38.p12 chr20: 23,637,688-23,638,483 CST3
    nsv4620572copy number variation1nstd183human GRCh37 chr20: 23,616,035-23,619,121 , GRCh38.p12 chr20: 23,635,398-23,638,484 CST3
    nsv4427813copy number variation1nstd174human GRCh37 chr20: 23,605,487-23,605,572 , GRCh38.p12 chr20: 23,624,850-23,624,935 CST3
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    nsv4336704sequence alteration1nstd166human GRCh37.p13 chr20: 8,105,854-23,795,733 , GRCh38.p12 chr20: 8,125,207-23,815,096 , BFSP1, 242 more genes
    nsv4286195copy number variation1nstd166human GRCh37.p13 chr20: 23,605,496-23,606,104 , GRCh38.p12 chr20: 23,624,859-23,625,467 CST3
    nsv4279744copy number variation1nstd166human GRCh37.p13 chr20: 23,374,022-24,054,368 , GRCh38.p12 chr20: 23,393,385-24,073,731 , CST3, 23 more genes
    nsv3923728copy number variation1nstd102humanUncertain significance NCBI36 chr20: 23,541,601-24,042,439 , GRCh37.p13 chr20: 23,593,601-24,094,439 , GRCh38.p12 chr20: 23,612,964-24,113,803 CSTP2, LOC107985438, 13 more genes
    nsv3922272copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103 ISM1-AS1, CST2, 498 more genes
    nsv3921497copy number variation1nstd102humanUncertain significance GRCh38 chr20: 23,455,996-24,050,737 , GRCh37 chr20: 23,436,633-24,031,374 , NCBI36 chr20: 23,384,633-23,979,374 CSTP1, CST9LP2, 19 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
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