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Items: 1 to 20 of 266

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097847copy number variation1nstd102humanPathogenic GRCh37 chr6: 7,582,865-7,586,121 , GRCh38.p12 chr6: 7,582,632-7,585,888 DSP
    nsv7097846copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 7,576,220-7,581,055 , GRCh38.p12 chr6: 7,575,987-7,580,822 DSP
    nsv7097454copy number variation1nstd102humanUncertain significance GRCh37 chr6: 7,542,149-7,880,576 , GRCh38.p12 chr6: 7,541,916-7,880,343 DSP-AS1, RPL29P1, 6 more genes
    nsv7097453copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 7,542,149-7,542,338 , GRCh38.p12 chr6: 7,541,916-7,542,105 DSP-AS1, DSP
    nsv7097089copy number variation1nstd102humanPathogenic GRCh37 chr6: 7,582,855-7,586,131 , GRCh38.p12 chr6: 7,582,622-7,585,898 DSP
    nsv7097088copy number variation1nstd102humanPathogenic GRCh37 chr6: 7,567,563-7,584,301 , GRCh38.p12 chr6: 7,567,330-7,584,068 DSP
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv6790498copy number variation1nstd229human GRCh38 chr6: 7,548,701-7,553,100 , GRCh37.p13 chr6: 7,548,934-7,553,333 DSP
    nsv6789765copy number variation1nstd229human GRCh38 chr6: 7,548,601-7,553,200 , GRCh37.p13 chr6: 7,548,834-7,553,433 DSP
    nsv6785945copy number variation1nstd229human GRCh38 chr6: 7,559,401-7,562,650 , GRCh37.p13 chr6: 7,559,634-7,562,883 DSP
    nsv6785440copy number variation1nstd229human GRCh38 chr6: 7,582,947-7,587,670 , GRCh37.p13 chr6: 7,583,180-7,587,903 DSP
    nsv6781517copy number variation1nstd229human GRCh38 chr6: 7,579,766-7,582,639 , GRCh37.p13 chr6: 7,579,999-7,582,872 DSP
    nsv6778316copy number variation1nstd229human GRCh38 chr6: 7,404,801-7,586,300 , GRCh37.p13 chr6: 7,405,034-7,586,533 RPS26P29, LOC102724234, 5 more genes
    nsv6414718copy number variation1nstd223human GRCh38 chr6: 7,551,457-7,552,492 , GRCh37.p13 chr6: 7,551,690-7,552,725 DSP
    nsv6409723copy number variation1nstd223human GRCh38 chr6: 7,366,072-12,459,745 , GRCh37.p13 chr6: 7,366,305-12,459,977 EEF1E1, RPS26P29, 82 more genes
    nsv6409276copy number variation1nstd223human GRCh38 chr6: 7,585,101-7,591,500 , GRCh37.p13 chr6: 7,585,334-7,591,733 DSP, SNRNP48
    nsv6399255copy number variation1nstd223human GRCh38 chr6: 7,548,640-7,553,136 , GRCh37.p13 chr6: 7,548,873-7,553,369 DSP
    nsv6314233delins1nstd102humanUncertain significance GRCh38 chr6: 7,584,805-7,584,806 , GRCh37 chr6: 7,585,038-7,585,039 DSP
    nsv6314225insertion1nstd102humanPathogenic GRCh37 chr6: 7,579,987-7,579,987 , GRCh38 chr6: 7,579,754-7,579,754 DSP
    nsv6312506copy number variation1nstd102humanUncertain significance GRCh37 chr6: 7,579,782-7,581,194 , GRCh38.p12 chr6: 7,579,549-7,580,961 DSP
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