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Items: 1 to 20 of 338

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978681insertion1nstd209human GRCh38 chr17: 42,265,377-42,265,377 , GRCh37.p13 chr17: 40,417,395-40,417,395 STAT5B
    nsv5972623insertion1nstd209human GRCh38 chr17: 42,198,929-42,198,929 , GRCh37.p13 chr17: 40,350,947-40,350,947 STAT5B
    nsv5944442copy number variation1nstd209human GRCh38 chr17: 42,238,413-42,238,711 , GRCh37.p13 chr17: 40,390,431-40,390,729 STAT5B
    nsv5940121copy number variation1nstd209human GRCh38 chr17: 42,199,227-42,199,278 , GRCh37.p13 chr17: 40,351,245-40,351,296 STAT5B
    nsv5937438copy number variation1nstd209human GRCh38 chr17: 42,213,740-42,213,966 , GRCh37.p13 chr17: 40,365,758-40,365,984 STAT5B
    nsv5882946copy number variation1nstd209human GRCh38 chr17: 42,246,750-42,248,749 , GRCh37.p13 chr17: 40,398,768-40,400,767 STAT5B
    nsv5714616mobile element insertion1nstd211human GRCh38 chr17: 42,265,389-42,265,389 , GRCh37.p13 chr17: 40,417,407-40,417,407 STAT5B
    nsv5657363insertion1nstd207human GRCh38 chr17: 42,224,982-42,224,982 , GRCh37.p13 chr17: 40,377,000-40,377,000 STAT5B
    nsv5562780sequence alteration1nstd206human GRCh38 chr17: 41,964,018-42,255,340 , GRCh37.p13 chr17|NW_003571052.1: 250,660-412,535 , GRCh37.p13 chr17: 40,116,036-40,277,911 KAT2A, STAT5B, 13 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5531546copy number variation1nstd206human GRCh38 chr17: 42,238,426-42,238,712 , GRCh37.p13 chr17: 40,390,444-40,390,730 STAT5B
    nsv5531042copy number variation1nstd206human GRCh38 chr17: 42,251,660-42,251,766 , GRCh37.p13 chr17: 40,403,678-40,403,784 STAT5B
    nsv5530698copy number variation1nstd206human GRCh38 chr17: 42,199,228-42,199,279 , GRCh37.p13 chr17: 40,351,246-40,351,297 STAT5B
    nsv5526736copy number variation1nstd206human GRCh38 chr17: 42,235,980-42,241,980 , GRCh37.p13 chr17: 40,387,998-40,393,998 STAT5B
    nsv5525274copy number variation1nstd206human GRCh38 chr17: 42,221,276-42,221,431 , GRCh37.p13 chr17: 40,373,294-40,373,449 STAT5B
    nsv5514789copy number variation1nstd206human GRCh38 chr17: 42,262,775-42,262,827 , GRCh37.p13 chr17: 40,414,793-40,414,845 STAT5B
    nsv5199568mobile element insertion1nstd203human GRCh38 chr17: 42,265,377-42,265,389 , GRCh37.p13 chr17: 40,417,395-40,417,407 STAT5B
    nsv5187293mobile element insertion1nstd203human GRCh38 chr17: 42,262,579-42,262,594 , GRCh37.p13 chr17: 40,414,597-40,414,612 STAT5B
    nsv5157501mobile element insertion1nstd203human GRCh38 chr17: 42,198,929-42,198,932 , GRCh37.p13 chr17: 40,350,947-40,350,950 STAT5B
    nsv5150902mobile element insertion1nstd203human GRCh38 chr17: 42,225,912-42,225,926 , GRCh37.p13 chr17: 40,377,930-40,377,944 STAT5B
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