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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131662insertion1nstd186human GRCh37 chr12: 117,513,760-117,513,760 , GRCh38.p12 chr12: 117,075,955-117,075,955 TESC
    nsv6130401insertion1nstd186human GRCh37 chr12: 117,494,187-117,494,236 , GRCh38.p12 chr12: 117,056,382-117,056,431 TESC
    nsv5977140insertion1nstd209human GRCh38 chr12: 117,056,380-117,056,380 , GRCh37.p13 chr12: 117,494,185-117,494,185 TESC
    nsv5938833copy number variation1nstd209human GRCh38 chr12: 117,082,917-117,083,535 , GRCh37.p13 chr12: 117,520,722-117,521,340 TESC
    nsv5860213copy number variation1nstd209human GRCh38 chr12: 117,051,282-117,053,956 , GRCh37.p13 chr12: 117,489,087-117,491,761 TESC
    nsv5702838mobile element insertion1nstd211human GRCh38 chr12: 117,037,663-117,037,663 , GRCh37.p13 chr12: 117,475,468-117,475,468 TESC
    nsv5661638insertion1nstd207human GRCh38 chr12: 117,056,380-117,056,380 , GRCh37.p13 chr12: 117,494,185-117,494,185 TESC
    nsv5596857copy number variation1nstd207human GRCh38 chr12: 117,056,122-117,056,257 , GRCh37.p13 chr12: 117,493,927-117,494,062 TESC
    nsv5586061copy number variation1nstd207human GRCh38 chr12: 117,075,868-117,075,984 , GRCh37.p13 chr12: 117,513,673-117,513,789 TESC
    nsv5551979insertion1nstd206human GRCh38 chr12: 117,056,382-117,056,431 , GRCh37.p13 chr12: 117,494,187-117,494,236 TESC
    nsv5535791insertion1nstd206human GRCh38 chr12: 117,075,955-117,075,955 , GRCh37.p13 chr12: 117,513,760-117,513,760 TESC
    nsv5505247copy number variation1nstd206human GRCh38 chr12: 117,082,921-117,083,536 , GRCh37.p13 chr12: 117,520,726-117,521,341 TESC
    nsv5422944mobile element insertion1nstd206human GRCh38 chr12: 117,037,663-117,037,690 , GRCh37.p13 chr12: 117,475,468-117,475,495 TESC
    nsv5356435translocation1nstd200human GRCh38 chr12: 117,082,921-117,082,921 , GRCh38 chr12: 117,083,536-117,083,536 , GRCh37.p13 chr12: 117,521,341-117,521,341 , GRCh37.p13 chr12: 117,520,726-117,520,726 TESC
    nsv5337874translocation1nstd200human GRCh37 chr12: 117,521,341-117,521,341 , GRCh37 chr12: 117,520,726-117,520,726 , GRCh38.p12 chr12: 117,082,921-117,082,921 , GRCh38.p12 chr12: 117,083,536-117,083,536 TESC
    nsv5326238translocation1nstd204human GRCh38.p13 chr12: 117,082,921-117,082,921 , GRCh38.p13 chr12: 117,083,536-117,083,536 , GRCh37.p13 chr12: 117,520,726-117,520,726 , GRCh37.p13 chr12: 117,521,341-117,521,341 TESC
    nsv5317341copy number variation1nstd204human GRCh38.p13 chr12: 117,080,299-117,081,724 , GRCh37.p13 chr12: 117,518,104-117,519,529 TESC
    nsv5303357copy number variation1nstd204human GRCh38.p13 chr12: 117,056,011-117,060,146 , GRCh37.p13 chr12: 117,493,816-117,497,951 TESC
    nsv5272419copy number variation1nstd204human GRCh38.p13 chr12: 117,082,431-117,083,630 , GRCh37.p13 chr12: 117,520,236-117,521,435 TESC
    nsv5272094copy number variation1nstd204human GRCh38.p13 chr12: 117,082,901-117,083,500 , GRCh37.p13 chr12: 117,520,706-117,521,305 TESC
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