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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5893389copy number variation1nstd209human GRCh38 chr6: 137,986,656-139,086,959 , GRCh37.p13 chr6: 138,307,793-139,408,096 ECT2L, NHSL1-AS1, 17 more genes
    nsv5641047insertion1nstd207human GRCh38 chr6: 138,775,842-138,775,842 , GRCh37.p13 chr6: 139,096,979-139,096,979 CCDC28A
    nsv5457404copy number variation1nstd206human GRCh38 chr6: 138,788,095-138,788,160 , GRCh37.p13 chr6: 139,109,232-139,109,297 CCDC28A
    nsv5369815translocation1nstd200human GRCh38 chr6: 138,788,095-138,788,095 , GRCh38 chr6: 138,788,160-138,788,160 , GRCh37.p13 chr6: 139,109,232-139,109,232 , GRCh37.p13 chr6: 139,109,297-139,109,297 CCDC28A
    nsv5369814translocation1nstd200human GRCh38 chr6: 138,785,275-138,785,275 , GRCh38 chr6: 138,785,328-138,785,328 , GRCh37.p13 chr6: 139,106,412-139,106,412 , GRCh37.p13 chr6: 139,106,465-139,106,465 CCDC28A
    nsv5363413translocation1nstd200human GRCh38 chr6: 138,774,453-138,774,453 , GRCh38 chr6: 139,048,126-139,048,126 , GRCh37.p13 chr6: 139,095,590-139,095,590 , GRCh37.p13 chr6: 139,369,263-139,369,263 CCDC28A
    nsv5339733translocation1nstd200human GRCh37 chr6: 139,106,465-139,106,465 , GRCh37 chr6: 139,106,412-139,106,412 , GRCh38.p12 chr6: 138,785,328-138,785,328 , GRCh38.p12 chr6: 138,785,275-138,785,275 CCDC28A
    nsv5335875translocation1nstd200human GRCh37 chr6: 139,369,263-139,369,263 , GRCh37 chr6: 139,095,590-139,095,590 , GRCh38.p12 chr6: 138,774,453-138,774,453 , GRCh38.p12 chr6: 139,048,126-139,048,126 CCDC28A
    nsv5302243copy number variation1nstd204human GRCh38.p13 chr6: 138,778,569-138,778,772 , GRCh37.p13 chr6: 139,099,706-139,099,909 CCDC28A
    nsv5236178copy number variation1nstd204human GRCh38.p13 chr6: 138,771,614-138,774,064 , GRCh37.p13 chr6: 139,092,751-139,095,201 CCDC28A-AS1, CCDC28A
    nsv5185340mobile element insertion1nstd203human GRCh38 chr6: 138,775,842-138,775,859 , GRCh37.p13 chr6: 139,096,979-139,096,996 CCDC28A
    nsv5039909inversion1nstd200human GRCh38 chr6: 137,955,606-139,947,661 , GRCh37.p13 chr6: 138,276,743-140,268,798 , CCDC28A-AS1, 30 more genes
    nsv4945729copy number variation1nstd200human GRCh38 chr6: 138,605,250-138,811,414 , GRCh37.p13 chr6: 138,926,387-139,132,551 ECT2L, NHSL1-AS1, 4 more genes
    nsv4824740copy number variation1nstd200human GRCh37 chr6: 138,926,387-139,132,551 , GRCh38.p12 chr6: 138,605,250-138,811,414 NHSL1-AS1, MTCH1P1, 4 more genes
    nsv4810584copy number variation1nstd200human GRCh37 chr6: 139,109,232-139,109,297 , GRCh38.p12 chr6: 138,788,095-138,788,160 CCDC28A
    nsv4810583copy number variation1nstd200human GRCh37 chr6: 139,099,732-139,099,885 , GRCh38.p12 chr6: 138,778,595-138,778,748 CCDC28A
    nsv4685709copy number variation1nstd102humannot provided GRCh37 chr6: 135,936,688-140,660,269 , GRCh38.p12 chr6: 135,615,550-140,339,132 MAP7, RN7SKP299, 74 more genes
    nsv4680132copy number variation1nstd189human GRCh37.p13 chr6: 138,484,930-139,143,192 , GRCh38.p12 chr6: 138,163,793-138,822,055 HEBP2, CCDC28A, 11 more genes
    nsv4678977copy number variation1nstd189human GRCh37.p13 chr6: 138,480,417-139,142,058 , GRCh38.p12 chr6: 138,159,280-138,820,921 HEBP2, CCDC28A, 11 more genes
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