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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903936copy number variation1nstd209human GRCh38 chr3: 44,378,897-44,385,479 , GRCh37.p13 chr3: 44,420,389-44,426,971 TCAIM
    nsv5897638copy number variation1nstd209human GRCh38 chr3: 44,340,617-44,345,350 , GRCh37.p13 chr3: 44,382,109-44,386,842 TCAIM
    nsv5836279copy number variation1nstd209human GRCh38 chr3: 44,378,639-44,385,138 , GRCh37.p13 chr3: 44,420,131-44,426,630 TCAIM
    nsv5835980copy number variation1nstd209human GRCh38 chr3: 44,340,635-44,345,302 , GRCh37.p13 chr3: 44,382,127-44,386,794 TCAIM
    nsv5451848copy number variation1nstd206human GRCh38 chr3: 44,340,603-44,345,351 , GRCh37.p13 chr3: 44,382,095-44,386,843 TCAIM
    nsv5447850copy number variation1nstd206human GRCh38 chr3: 44,345,671-44,348,897 , GRCh37.p13 chr3: 44,387,163-44,390,389 TCAIM
    nsv5443247copy number variation1nstd206human GRCh38 chr3: 44,378,897-44,385,507 , GRCh37.p13 chr3: 44,420,389-44,426,999 TCAIM
    nsv5377476translocation1nstd200human GRCh38 chr3: 44,385,481-44,385,481 , GRCh38 chr3: 44,379,021-44,379,021 , GRCh37.p13 chr3: 44,420,513-44,420,513 , GRCh37.p13 chr3: 44,426,973-44,426,973 TCAIM
    nsv5351718translocation1nstd200human GRCh38 chr3: 44,340,603-44,340,603 , GRCh38 chr3: 44,345,351-44,345,351 , GRCh37.p13 chr3: 44,386,843-44,386,843 , GRCh37.p13 chr3: 44,382,095-44,382,095 TCAIM
    nsv5318528copy number variation1nstd204human GRCh38.p13 chr3: 44,378,872-44,385,531 , GRCh37.p13 chr3: 44,420,364-44,427,023 TCAIM
    nsv5214850copy number variation1nstd204human GRCh38.p13 chr3: 44,378,701-44,384,500 , GRCh37.p13 chr3: 44,420,193-44,425,992 TCAIM
    nsv5206091copy number variation1nstd204human GRCh38.p13 chr3: 44,378,639-44,385,113 , GRCh37.p13 chr3: 44,420,131-44,426,605 TCAIM
    nsv5204563copy number variation1nstd204human GRCh38.p13 chr3: 44,377,727-44,386,050 , GRCh37.p13 chr3: 44,419,219-44,427,542 TCAIM
    nsv5076947mobile element insertion1nstd203human GRCh38 chr3: 44,343,200-44,343,212 , GRCh37.p13 chr3: 44,384,692-44,384,704 TCAIM
    nsv5063300mobile element insertion1nstd203human GRCh38 chr3: 44,395,689-44,395,706 , GRCh37.p13 chr3: 44,437,181-44,437,198 TCAIM
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924380copy number variation1nstd200human GRCh38 chr3: 44,379,028-44,385,818 , GRCh37.p13 chr3: 44,420,520-44,427,310 TCAIM
    nsv4924379copy number variation1nstd200human GRCh38 chr3: 44,378,897-44,385,508 , GRCh37.p13 chr3: 44,420,389-44,427,000 TCAIM
    nsv4911050copy number variation1nstd200human GRCh38 chr3: 44,372,969-44,373,152 , GRCh37.p13 chr3: 44,414,461-44,414,644 TCAIM
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