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Items: 1 to 20 of 337

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967053insertion1nstd209human GRCh38 chr7: 26,469,984-26,469,984 , GRCh37.p13 chr7: 26,509,604-26,509,604 LINC02981
    nsv5926123copy number variation1nstd209human GRCh38 chr7: 26,469,640-26,469,939 , GRCh37.p13 chr7: 26,509,260-26,509,559 LINC02981
    nsv5919512copy number variation1nstd209human GRCh38 chr7: 26,509,679-33,120,288 , GRCh37.p13 chr7: 26,549,298-33,159,900 , CPVL-AS1, 126 more genes
    nsv5678147mobile element insertion2nstd211human GRCh38 chr7: 26,453,348-26,453,348 , GRCh37.p13 chr7: 26,492,968-26,492,968 LINC02981
    nsv5637536insertion1nstd207human GRCh38 chr7: 26,469,976-26,469,976 , GRCh37.p13 chr7: 26,509,596-26,509,596 LINC02981
    nsv5566370copy number variation1nstd207human GRCh38 chr7: 26,469,640-26,469,897 , GRCh37.p13 chr7: 26,509,260-26,509,517 LINC02981
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5488408copy number variation1nstd206human GRCh38 chr7: 26,469,640-26,470,025 , GRCh37.p13 chr7: 26,509,260-26,509,645 LINC02981
    nsv5477743copy number variation1nstd206human GRCh38 chr7: 26,461,574-26,461,832 , GRCh37.p13 chr7: 26,501,194-26,501,452 LINC02981
    nsv5476595copy number variation1nstd206human GRCh38 chr7: 26,527,576-26,527,652 , GRCh37.p13 chr7: 26,567,195-26,567,271 LINC02981
    nsv5476283copy number variation1nstd206human GRCh38 chr7: 26,515,328-26,515,708 , GRCh37.p13 chr7: 26,554,947-26,555,327 LINC02981
    nsv5400053mobile element insertion1nstd206human GRCh38 chr7: 26,453,348-26,453,399 , GRCh37.p13 chr7: 26,492,968-26,493,019 LINC02981
    nsv5389334copy number variation1nstd186human GRCh37 chr7: 26,509,261-26,509,594 , GRCh38.p12 chr7: 26,469,641-26,469,974 LINC02981
    nsv5370468translocation1nstd200human GRCh38 chr7: 26,466,140-26,466,140 , GRCh38 chr7: 26,466,690-26,466,690 , GRCh37.p13 chr7: 26,505,760-26,505,760 , GRCh37.p13 chr7: 26,506,310-26,506,310 LINC02981
    nsv5370467translocation1nstd200human GRCh38 chr7: 26,411,046-26,411,046 , GRCh38 chr7: 26,411,108-26,411,108 , GRCh37.p13 chr7: 26,450,666-26,450,666 , GRCh37.p13 chr7: 26,450,728-26,450,728 LINC02981
    nsv5330808translocation1nstd200human GRCh37 chr7: 26,440,951-26,440,951 , GRCh37 chr7: 26,425,050-26,425,050 , GRCh38.p12 chr7: 26,385,430-26,385,430 , GRCh38.p12 chr7: 26,401,331-26,401,331 LINC02981, SNX10-AS1
    nsv5309075copy number variation1nstd204human GRCh38.p13 chr7: 26,515,318-26,515,709 , GRCh37.p13 chr7: 26,554,937-26,555,328 LINC02981
    nsv5308352copy number variation1nstd204human GRCh38.p13 chr7: 26,469,630-26,469,992 , GRCh37.p13 chr7: 26,509,250-26,509,612 LINC02981
    nsv5222735copy number variation1nstd204human GRCh38.p13 chr7: 26,469,701-26,469,900 , GRCh37.p13 chr7: 26,509,321-26,509,520 LINC02981
    nsv5217031mobile element deletion1nstd204human GRCh38.p13 chr7: 26,407,954-26,408,312 , GRCh37.p13 chr7: 26,447,574-26,447,932 LINC02981
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