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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5337177translocation1nstd200human GRCh37 chr20: 5,104,566-5,104,566 , GRCh37 chr20: 5,108,845-5,108,845 , GRCh38.p12 chr20: 5,123,920-5,123,920 , GRCh38.p12 chr20: 5,128,199-5,128,199 CDS2, PCNA
    nsv5287442copy number variation1nstd204human GRCh38.p13 chr20: 5,032,301-5,164,000 , GRCh37.p13 chr20: 5,012,947-5,144,646 PCNA-AS1, CDS2, 3 more genes
    nsv5175087mobile element insertion1nstd203human GRCh38 chr20: 5,125,527-5,125,543 , GRCh37.p13 chr20: 5,106,173-5,106,189 CDS2, PCNA
    nsv5033561inversion1nstd200human GRCh38 chr20: 3,693,712-5,966,244 , GRCh37.p13 chr20: 3,674,359-5,946,890 , LOC107985411, 53 more genes
    nsv4680516copy number variation1nstd189human GRCh37.p13 chr20: 5,032,137-5,294,133 , GRCh38.p12 chr20: 5,051,491-5,313,487 PCNA, CDS2, 5 more genes
    nsv4679957copy number variation1nstd189human GRCh37.p13 chr20: 5,038,963-5,253,429 , GRCh38.p12 chr20: 5,058,317-5,272,783 PCNA, CDS2, 3 more genes
    nsv4679835copy number variation1nstd189human GRCh37.p13 chr20: 5,032,137-5,253,429 , GRCh38.p12 chr20: 5,051,491-5,272,783 PCNA, CDS2, 3 more genes
    nsv4678920copy number variation1nstd189human GRCh37.p13 chr20: 5,032,137-5,330,915 , GRCh38.p12 chr20: 5,051,491-5,350,269 PCNA, CDS2, 6 more genes
    nsv4631248copy number variation1nstd183human GRCh37 chr20: 5,093,200-5,113,940 , GRCh38.p12 chr20: 5,112,554-5,133,294 PCNA-AS1, PCNA, 2 more genes
    nsv4629477copy number variation1nstd183human GRCh37 chr20: 4,963,827-5,644,184 , GRCh38.p12 chr20: 4,983,181-5,663,538 , LOC107985411, 17 more genes
    nsv4628873copy number variation1nstd183human GRCh37 chr20: 5,099,321-5,099,548 , GRCh38.p12 chr20: 5,118,675-5,118,902 PCNA, PCNA-AS1
    nsv4623505copy number variation1nstd183human GRCh37 chr20: 5,107,035-5,107,502 , GRCh38.p12 chr20: 5,126,389-5,126,856 CDS2, PCNA
    nsv4502972mobile element insertion1nstd166human GRCh37.p13 chr20: 5,106,173-5,106,173 , GRCh38.p12 chr20: 5,125,527-5,125,527 CDS2, PCNA
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    nsv4330625inversion1nstd166human GRCh37.p13 chr20: 2,496,151-5,491,306 , GRCh38.p12 chr20: 2,515,505-5,510,660 , ADRA1D, 89 more genes
    nsv3923490copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-13,029,401 , NCBI36 chr20: 8,747-12,958,049 , GRCh37 chr20: 60,747-13,010,049 LINC01751, RNA5SP474, 238 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
    nsv3922038copy number variation1nstd102humanUncertain significance GRCh38 chr20: 80,927-5,447,679 , NCBI36 chr20: 9,568-5,376,325 , GRCh37 chr20: 61,568-5,428,325 LOC105372509, SIRPD, 150 more genes
    nsv3921972copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-19,074,923 , GRCh38 chr20: 89,939-19,146,279 , GRCh37 chr20: 70,580-19,126,923 PTMAP3, LOC105372517, 331 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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