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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923787copy number variation1nstd209human GRCh38 chr7: 55,368,625-55,368,703 , GRCh37.p13 chr7: 55,436,318-55,436,396 LANCL2
    nsv5577355copy number variation1nstd207human GRCh38 chr7: 55,368,624-55,368,702 , GRCh37.p13 chr7: 55,436,317-55,436,395 LANCL2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5487234copy number variation1nstd206human GRCh38 chr7: 55,408,275-55,408,451 , GRCh37.p13 chr7: 55,475,968-55,476,144 LANCL2
    nsv5484824copy number variation1nstd206human GRCh38 chr7: 55,390,460-55,390,604 , GRCh37.p13 chr7: 55,458,153-55,458,297 LANCL2
    nsv5477559copy number variation1nstd206human GRCh38 chr7: 55,368,625-55,368,705 , GRCh37.p13 chr7: 55,436,318-55,436,398 LANCL2
    nsv5477528copy number variation1nstd206human GRCh38 chr7: 55,282,120-56,410,000 , GRCh37.p13 chr7: 55,349,813-56,477,693 , MRPS17, 52 more genes
    nsv5370581translocation1nstd200human GRCh38 chr7: 55,392,900-55,392,900 , GRCh38 chr7: 55,387,488-55,387,488 , GRCh37.p13 chr7: 55,455,181-55,455,181 , GRCh37.p13 chr7: 55,460,593-55,460,593 LANCL2
    nsv5370580translocation1nstd200human GRCh38 chr7: 55,387,471-55,387,471 , GRCh38 chr7: 55,393,730-55,393,730 , GRCh37.p13 chr7: 55,455,164-55,455,164 , GRCh37.p13 chr7: 55,461,423-55,461,423 LANCL2
    nsv5363688translocation1nstd200human GRCh38 chr7: 55,368,705-55,368,705 , GRCh38 chr7: 55,368,625-55,368,625 , GRCh37.p13 chr7: 55,436,398-55,436,398 , GRCh37.p13 chr7: 55,436,318-55,436,318 LANCL2
    nsv5341379translocation1nstd200human GRCh37 chr7: 55,448,891-55,448,891 , GRCh37 chr7: 55,619,543-55,619,543 , GRCh38.p12 chr7: 55,381,198-55,381,198 , GRCh38.p12 chr7: 55,551,850-55,551,850 VOPP1, LANCL2
    nsv5185136mobile element insertion1nstd203human GRCh38 chr7: 55,401,539-55,401,539 , GRCh37.p13 chr7: 55,469,232-55,469,232 LANCL2
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964658copy number variation1nstd200human GRCh38 chr7: 55,425,274-55,425,435 , GRCh37.p13 chr7: 55,492,967-55,493,128 LANCL2
    nsv4956824copy number variation1nstd200human GRCh38 chr7: 55,408,275-55,408,451 , GRCh37.p13 chr7: 55,475,968-55,476,144 LANCL2
    nsv4956823copy number variation1nstd200human GRCh38 chr7: 55,400,350-55,400,467 , GRCh37.p13 chr7: 55,468,043-55,468,160 LANCL2
    nsv4956822copy number variation1nstd200human GRCh38 chr7: 55,361,252-55,363,898 , GRCh37.p13 chr7: 55,428,945-55,431,591 LANCL2
    nsv4819018copy number variation1nstd200human GRCh37 chr7: 55,428,945-55,431,591 , GRCh38.p12 chr7: 55,361,252-55,363,898 LANCL2
    nsv4732664copy number variation1nstd199human GRCh37 chr7: 55,458,260-55,458,436 , GRCh38.p12 chr7: 55,390,567-55,390,743 LANCL2
    nsv4709251copy number variation1nstd195human GRCh37 chr7: 55,471,201-55,521,901 , GRCh38.p12 chr7: 55,403,508-55,454,208 LANCL2, VOPP1
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