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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127384insertion1nstd186human GRCh37 chr12: 67,705,322-67,705,363 , GRCh38.p12 chr12: 67,311,542-67,311,583 CAND1
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5944209copy number variation1nstd209human GRCh38 chr12: 67,296,230-67,296,298 , GRCh37.p13 chr12: 67,690,010-67,690,078 CAND1
    nsv5943949copy number variation1nstd209human GRCh38 chr12: 67,284,711-67,284,793 , GRCh37.p13 chr12: 67,678,491-67,678,573 CAND1
    nsv5939815copy number variation1nstd209human GRCh38 chr12: 67,278,515-67,279,700 , GRCh37.p13 chr12: 67,672,295-67,673,480 CAND1
    nsv5697588mobile element insertion2nstd211human GRCh38 chr12: 67,274,182-67,274,182 , GRCh37.p13 chr12: 67,667,962-67,667,962 CAND1
    nsv5661198insertion1nstd207human GRCh38 chr12: 67,311,532-67,311,532 , GRCh37.p13 chr12: 67,705,312-67,705,312 CAND1
    nsv5655429insertion1nstd207human GRCh38 chr12: 67,284,711-67,284,711 , GRCh37.p13 chr12: 67,678,491-67,678,491 CAND1
    nsv5546396insertion1nstd206human GRCh38 chr12: 67,284,726-67,284,762 , GRCh37.p13 chr12: 67,678,506-67,678,542 CAND1
    nsv5543136insertion1nstd206human GRCh38 chr12: 67,311,542-67,311,583 , GRCh37.p13 chr12: 67,705,322-67,705,363 CAND1
    nsv5506386copy number variation1nstd206human GRCh38 chr12: 67,276,938-67,279,126 , GRCh37.p13 chr12: 67,670,718-67,672,906 CAND1
    nsv5498145copy number variation1nstd206human GRCh38 chr12: 67,294,787-67,294,839 , GRCh37.p13 chr12: 67,688,567-67,688,619 CAND1
    nsv5495019copy number variation1nstd206human GRCh38 chr12: 67,263,151-67,356,199 , GRCh37.p13 chr12: 67,656,931-67,749,979 GGTA2P, CAND1, 1 more genes
    nsv5494711copy number variation1nstd206human GRCh38 chr12: 67,296,230-67,296,293 , GRCh37.p13 chr12: 67,690,010-67,690,073 CAND1
    nsv5428675mobile element insertion1nstd206human GRCh38 chr12: 67,274,182-67,274,233 , GRCh37.p13 chr12: 67,667,962-67,668,013 CAND1
    nsv5374055translocation1nstd200human GRCh38 chr12: 67,278,246-67,278,246 , GRCh38 chr12: 67,279,693-67,279,693 , GRCh37.p13 chr12: 67,672,026-67,672,026 , GRCh37.p13 chr12: 67,673,473-67,673,473 CAND1
    nsv5356053translocation1nstd200human GRCh38 chr12: 67,278,516-67,278,516 , GRCh38 chr12: 67,279,701-67,279,701 , GRCh37.p13 chr12: 67,672,296-67,672,296 , GRCh37.p13 chr12: 67,673,481-67,673,481 CAND1
    nsv5342484translocation1nstd200human GRCh37 chr12: 67,672,296-67,672,296 , GRCh37 chr12: 67,673,481-67,673,481 , GRCh38.p12 chr12: 67,279,701-67,279,701 , GRCh38.p12 chr12: 67,278,516-67,278,516 CAND1
    nsv5333874translocation1nstd200human GRCh37 chr12: 67,672,026-67,672,026 , GRCh37 chr12: 67,673,473-67,673,473 , GRCh38.p12 chr12: 67,278,246-67,278,246 , GRCh38.p12 chr12: 67,279,693-67,279,693 CAND1
    nsv5321295translocation1nstd204human GRCh38.p13 chr12: 67,278,516-67,278,516 , GRCh38.p13 chr12: 67,279,701-67,279,701 , GRCh37.p13 chr12: 67,673,481-67,673,481 , GRCh37.p13 chr12: 67,672,296-67,672,296 CAND1
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