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Items: 1 to 20 of 1859

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137701copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 28,669,064-31,367,407 , GRCh38.p12 chr13: 28,094,927-30,793,270 ALOX5AP, FLT1, 41 more genes
    nsv6131707insertion1nstd186human GRCh37 chr13: 29,564,787-29,564,815 , GRCh38.p12 chr13: 28,990,650-28,990,678 MTUS2
    nsv6122518copy number variation1nstd186human GRCh37 chr13: 29,722,260-29,722,915 , GRCh38.p12 chr13: 29,148,123-29,148,778 MTUS2
    nsv6122331copy number variation1nstd186human GRCh37 chr13: 29,478,243-29,483,966 , GRCh38.p12 chr13: 28,904,106-28,909,829 MTUS2
    nsv6121402copy number variation1nstd186human GRCh37 chr13: 29,722,610-29,722,914 , GRCh38.p12 chr13: 29,148,473-29,148,777 MTUS2
    nsv6121025copy number variation1nstd186human GRCh37 chr13: 29,564,998-29,565,136 , GRCh38.p12 chr13: 28,990,861-28,990,999 MTUS2
    nsv6116692mobile element insertion1nstd186human GRCh37 chr13: 29,412,102-29,412,153 , GRCh38.p12 chr13: 28,837,965-28,838,016 MTUS2
    nsv6114614mobile element insertion1nstd186human GRCh37 chr13: 29,538,875-29,538,875 , GRCh38.p12 chr13: 28,964,738-28,964,738 MTUS2
    nsv6114043mobile element insertion1nstd186human GRCh37 chr13: 30,031,568-30,031,568 , GRCh38.p12 chr13: 29,457,431-29,457,431 MTUS2
    nsv6112810copy number variation1nstd102humanPathogenic GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559 MTUS2, ALOX5AP, 70 more genes
    nsv5979389insertion1nstd209human GRCh38 chr13: 29,318,391-29,318,391 , GRCh37.p13 chr13: 29,892,528-29,892,528 MTUS2
    nsv5976037insertion1nstd209human GRCh38 chr13: 29,389,341-29,389,341 , GRCh37.p13 chr13: 29,963,478-29,963,478 MTUS2
    nsv5975179insertion1nstd209human GRCh38 chr13: 29,446,434-29,446,434 , GRCh37.p13 chr13: 30,020,571-30,020,571 MTUS2
    nsv5973841insertion1nstd209human GRCh38 chr13: 28,852,900-28,852,900 , GRCh37.p13 chr13: 29,427,037-29,427,037 MTUS2
    nsv5972163insertion1nstd209human GRCh38 chr13: 29,244,955-29,244,955 , GRCh37.p13 chr13: 29,819,092-29,819,092 MTUS2
    nsv5970480inversion1nstd209human GRCh38 chr13: 29,131,093-29,134,038 , GRCh37.p13 chr13: 29,705,230-29,708,175 MTUS2
    nsv5969729insertion1nstd209human GRCh38 chr13: 28,990,627-28,990,627 , GRCh37.p13 chr13: 29,564,764-29,564,764 MTUS2
    nsv5968185insertion1nstd209human GRCh38 chr13: 29,457,431-29,457,431 , GRCh37.p13 chr13: 30,031,568-30,031,568 MTUS2
    nsv5947279copy number variation1nstd209human GRCh38 chr13: 29,300,559-29,300,625 , GRCh37.p13 chr13: 29,874,696-29,874,762 MTUS2
    nsv5946813copy number variation1nstd209human GRCh38 chr13: 29,341,196-29,345,944 , GRCh37.p13 chr13: 29,915,333-29,920,081 MTUS2
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