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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916676copy number variation1nstd209human GRCh38 chr10: 88,881,414-88,881,559 , GRCh37.p13 chr10: 90,641,171-90,641,316 STAMBPL1
    nsv5700217mobile element insertion1nstd211human GRCh38 chr10: 88,888,989-88,888,989 , GRCh37.p13 chr10: 90,648,746-90,648,746 STAMBPL1
    nsv5700000mobile element insertion1nstd211human GRCh38 chr10: 88,904,861-88,904,861 , GRCh37.p13 chr10: 90,664,618-90,664,618 STAMBPL1
    nsv5540754insertion1nstd206human GRCh38 chr10: 88,888,989-88,889,036 , GRCh37.p13 chr10: 90,648,746-90,648,793 STAMBPL1
    nsv5488845copy number variation1nstd206human GRCh38 chr10: 88,881,415-88,881,560 , GRCh37.p13 chr10: 90,641,172-90,641,317 STAMBPL1
    nsv5484654copy number variation1nstd206human GRCh38 chr10: 88,357,217-89,008,458 , GRCh37.p13 chr10: 90,116,974-90,768,215 , RCBTB2P1, 17 more genes
    nsv5409659mobile element insertion1nstd206human GRCh38 chr10: 88,904,861-88,904,912 , GRCh37.p13 chr10: 90,664,618-90,664,669 STAMBPL1
    nsv5340259translocation1nstd200human GRCh37 chr10: 90,641,317-90,641,317 , GRCh37 chr10: 90,641,172-90,641,172 , GRCh38.p12 chr10: 88,881,415-88,881,415 , GRCh38.p12 chr10: 88,881,560-88,881,560 STAMBPL1
    nsv5135417mobile element insertion1nstd203human GRCh38 chr10: 88,917,466-88,917,482 , GRCh37.p13 chr10: 90,677,223-90,677,239 STAMBPL1
    nsv5120671mobile element insertion1nstd203human GRCh38 chr10: 88,904,850-88,904,861 , GRCh37.p13 chr10: 90,664,607-90,664,618 STAMBPL1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986553copy number variation1nstd200human GRCh38 chr10: 88,896,618-88,902,329 , GRCh37.p13 chr10: 90,656,375-90,662,086 STAMBPL1
    nsv4986552copy number variation1nstd200human GRCh38 chr10: 88,881,415-88,881,560 , GRCh37.p13 chr10: 90,641,172-90,641,317 STAMBPL1
    nsv4838940copy number variation1nstd200human GRCh37 chr10: 90,116,974-90,768,215 , GRCh38.p12 chr10: 88,357,217-89,008,458 , RNLS, 17 more genes
    nsv4729624copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,685,387-92,144,296 , GRCh38.p12 chr10: 86,925,630-90,384,539 LOC105378414, RN7SL78P, 84 more genes
    nsv4728982copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,122,675-90,771,228 , GRCh38.p12 chr10: 88,362,918-89,011,471 LIPJ, PTCD2P2, 16 more genes
    nsv4682162copy number variation1nstd102humanPathogenic GRCh37 chr10: 90,530,602-91,087,835 , GRCh38.p12 chr10: 88,770,845-89,328,078 MIR4679-2, ACTA2-AS1, 17 more genes
    nsv4681949copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,622,918-90,708,693 , GRCh38.p12 chr10: 87,863,161-88,948,936 LIPM, LIPJ, 22 more genes
    nsv4613470copy number variation1nstd183human GRCh37 chr10: 90,660,806-90,661,425 , GRCh38.p12 chr10: 88,901,049-88,901,668 STAMBPL1
    nsv4560739mobile element insertion1nstd166human GRCh37.p13 chr10: 90,657,397-90,657,397 , GRCh38.p12 chr10: 88,897,640-88,897,640 STAMBPL1
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