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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968549insertion1nstd209human GRCh38 chr20: 49,065,313-49,065,313 , GRCh37.p13 chr20: 47,681,850-47,681,850 CSE1L
    nsv5885318copy number variation1nstd209human GRCh38 chr20: 49,090,005-49,118,647 , GRCh37.p13 chr20: 47,706,542-47,735,184 STAU1, CSE1L
    nsv5715635mobile element insertion2nstd211human GRCh38 chr20: 49,093,244-49,093,244 , GRCh37.p13 chr20: 47,709,781-47,709,781 CSE1L
    nsv5703373mobile element insertion1nstd211human GRCh38 chr20: 49,053,171-49,053,171 , GRCh37.p13 chr20: 47,669,708-47,669,708 CSE1L
    nsv5554491mobile element insertion1nstd206human GRCh38 chr20: 49,093,244-49,093,295 , GRCh37.p13 chr20: 47,709,781-47,709,832 CSE1L
    nsv5519794copy number variation1nstd206human GRCh38 chr20: 49,089,625-49,130,812 , GRCh37.p13 chr20: 47,706,162-47,747,349 STAU1, CSE1L
    nsv5366145translocation1nstd200human GRCh38 chr20: 49,089,981-49,089,981 , GRCh38 chr20: 52,311,111-52,311,111 , GRCh37.p13 chr20: 47,706,518-47,706,518 , GRCh37.p13 chr20: 50,927,650-50,927,650 LOC105372666, CSE1L
    nsv5366144translocation1nstd200human GRCh38 chr20: 49,080,414-49,080,414 , GRCh38 chr20: 50,933,723-50,933,723 , GRCh37.p13 chr20: 47,696,951-47,696,951 , GRCh37.p13 chr20: 49,550,260-49,550,260 CSE1L, DPM1, 1 more genes
    nsv5350435translocation1nstd200human GRCh38 chr20: 48,936,110-48,936,110 , GRCh38 chr20: 49,055,936-49,055,936 , GRCh37.p13 chr20: 47,672,473-47,672,473 , GRCh37.p13 chr20: 47,552,647-47,552,647 ARFGEF2, CSE1L
    nsv5179735mobile element insertion1nstd203human GRCh38 chr20: 49,065,313-49,065,340 , GRCh37.p13 chr20: 47,681,850-47,681,877 CSE1L
    nsv5174237mobile element insertion1nstd203human GRCh38 chr20: 49,065,296-49,065,340 , GRCh37.p13 chr20: 47,681,833-47,681,877 CSE1L
    nsv5173337mobile element insertion1nstd203human GRCh38 chr20: 49,066,734-49,066,748 , GRCh37.p13 chr20: 47,683,271-47,683,285 CSE1L
    nsv5171110mobile element insertion1nstd203human GRCh38 chr20: 49,065,612-49,065,612 , GRCh37.p13 chr20: 47,682,149-47,682,149 CSE1L
    nsv5163239mobile element insertion1nstd203human GRCh38 chr20: 49,077,172-49,077,201 , GRCh37.p13 chr20: 47,693,709-47,693,738 CSE1L
    nsv5161429mobile element insertion1nstd203human GRCh38 chr20: 49,047,564-49,047,592 , GRCh37.p13 chr20: 47,664,101-47,664,129 CSE1L
    nsv5160130mobile element insertion1nstd203human GRCh38 chr20: 49,047,592-49,047,592 , GRCh37.p13 chr20: 47,664,129-47,664,129 CSE1L
    nsv4681865copy number variation1nstd102humanUncertain significance GRCh37 chr20: 47,538,407-48,099,037 , GRCh38.p12 chr20: 48,921,870-49,482,500 ARFGEF2, LOC105372649, 12 more genes
    nsv4629347copy number variation1nstd183human GRCh37 chr20: 47,653,070-47,665,757 , GRCh38.p12 chr20: 49,036,533-49,049,220 CSE1L, ARFGEF2, 2 more genes
    nsv4575609mobile element insertion1nstd166human GRCh37.p13 chr20: 47,709,767-47,709,767 , GRCh38.p12 chr20: 49,093,230-49,093,230 CSE1L
    nsv4508817mobile element insertion1nstd166human GRCh37.p13 chr20: 47,701,318-47,701,318 , GRCh38.p12 chr20: 49,084,781-49,084,781 CSE1L
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