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Items: 1 to 20 of 318

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978883inversion1nstd209human GRCh38 chr8: 124,481,433-124,485,057 , GRCh37.p13 chr8: 125,493,674-125,497,298 RNF139
    nsv5926484copy number variation1nstd209human GRCh38 chr8: 124,482,921-124,485,138 , GRCh37.p13 chr8: 125,495,162-125,497,379 RNF139
    nsv5918464copy number variation1nstd209human GRCh38 chr8: 124,480,155-124,483,072 , GRCh37.p13 chr8: 125,492,396-125,495,313 RNF139
    nsv5909798copy number variation1nstd209human GRCh38 chr8: 124,482,003-124,485,037 , GRCh37.p13 chr8: 125,494,244-125,497,278 RNF139
    nsv5908531copy number variation1nstd209human GRCh38 chr8: 124,480,375-124,485,334 , GRCh37.p13 chr8: 125,492,616-125,497,575 RNF139
    nsv5860697copy number variation1nstd209human GRCh38 chr8: 124,480,368-124,482,694 , GRCh37.p13 chr8: 125,492,609-125,494,935 RNF139
    nsv5859631copy number variation1nstd209human GRCh38 chr8: 124,481,795-124,482,794 , GRCh37.p13 chr8: 125,494,036-125,495,035 RNF139
    nsv5853881copy number variation1nstd209human GRCh38 chr8: 124,483,127-124,485,076 , GRCh37.p13 chr8: 125,495,368-125,497,317 RNF139
    nsv5641962insertion2nstd207human GRCh38 chr8: 124,483,113-124,483,113 , GRCh37.p13 chr8: 125,495,354-125,495,354 RNF139
    nsv5627502insertion1nstd207human GRCh38 chr8: 124,483,013-124,483,013 , GRCh37.p13 chr8: 125,495,254-125,495,254 RNF139
    nsv5581126copy number variation1nstd207human GRCh38 chr8: 124,482,947-124,483,112 , GRCh37.p13 chr8: 125,495,188-125,495,353 RNF139
    nsv5556077sequence alteration1nstd206human GRCh38 chr8: 124,481,432-124,485,058 , GRCh37.p13 chr8: 125,493,673-125,497,299 RNF139
    nsv5534385insertion1nstd206human GRCh38 chr8: 124,483,688-124,483,739 , GRCh37.p13 chr8: 125,495,929-125,495,980 RNF139
    nsv5487563copy number variation1nstd206human GRCh38 chr8: 124,478,000-124,483,000 , GRCh37.p13 chr8: 125,490,241-125,495,241 RNF139
    nsv5484967copy number variation1nstd206human GRCh38 chr8: 124,481,415-124,483,088 , GRCh37.p13 chr8: 125,493,656-125,495,329 RNF139
    nsv5481799copy number variation1nstd206human GRCh38 chr8: 124,480,467-124,488,186 , GRCh37.p13 chr8: 125,492,708-125,500,427 RNF139, TATDN1
    nsv5481556copy number variation1nstd206human GRCh38 chr8: 124,480,739-124,484,389 , GRCh37.p13 chr8: 125,492,980-125,496,630 RNF139
    nsv5479389copy number variation1nstd206human GRCh38 chr8: 124,481,665-124,484,213 , GRCh37.p13 chr8: 125,493,906-125,496,454 RNF139
    nsv5479034copy number variation1nstd206human GRCh38 chr8: 124,481,215-124,485,222 , GRCh37.p13 chr8: 125,493,456-125,497,463 RNF139
    nsv5475448copy number variation1nstd206human GRCh38 chr8: 124,483,114-124,485,756 , GRCh37.p13 chr8: 125,495,355-125,497,997 RNF139
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