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Items: 1 to 20 of 330

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977539insertion1nstd209human GRCh38 chr14: 31,199,322-31,199,322 , GRCh37.p13 chr14: 31,668,528-31,668,528 HECTD1
    nsv5972662insertion1nstd209human GRCh38 chr14: 31,142,753-31,142,753 , GRCh37.p13 chr14: 31,611,959-31,611,959 RNU6-541P, HECTD1
    nsv5969185insertion1nstd209human GRCh38 chr14: 31,134,042-31,134,042 , GRCh37.p13 chr14: 31,603,248-31,603,248 HECTD1
    nsv5727638mobile element insertion1nstd211human GRCh38 chr14: 31,111,179-31,111,179 , GRCh37.p13 chr14: 31,580,385-31,580,385 RPL21P5, HECTD1
    nsv5719205mobile element insertion1nstd211human GRCh38 chr14: 31,190,473-31,190,473 , GRCh37.p13 chr14: 31,659,679-31,659,679 HECTD1
    nsv5702507mobile element insertion2nstd211human GRCh38 chr14: 31,142,767-31,142,767 , GRCh37.p13 chr14: 31,611,973-31,611,973 RNU6-541P, HECTD1
    nsv5701556mobile element insertion2nstd211human GRCh38 chr14: 31,199,339-31,199,339 , GRCh37.p13 chr14: 31,668,545-31,668,545 HECTD1
    nsv5561412mobile element insertion1nstd206human GRCh38 chr14: 31,190,482-31,190,524 , GRCh37.p13 chr14: 31,659,688-31,659,730 HECTD1
    nsv5503060copy number variation1nstd206human GRCh38 chr14: 31,124,644-31,124,700 , GRCh37.p13 chr14: 31,593,850-31,593,906 HECTD1
    nsv5496932copy number variation1nstd206human GRCh38 chr14: 31,192,692-31,193,666 , GRCh37.p13 chr14: 31,661,898-31,662,872 HECTD1
    nsv5495631copy number variation1nstd206human GRCh38 chr14: 31,203,986-31,204,065 , GRCh37.p13 chr14: 31,673,192-31,673,271 HECTD1
    nsv5426492mobile element insertion1nstd206human GRCh38 chr14: 31,199,322-31,199,322 , GRCh37.p13 chr14: 31,668,528-31,668,528 HECTD1
    nsv5374477translocation1nstd200human GRCh38 chr14: 31,162,077-31,162,077 , GRCh38 chr14: 31,161,789-31,161,789 , GRCh37.p13 chr14: 31,631,283-31,631,283 , GRCh37.p13 chr14: 31,630,995-31,630,995 HECTD1
    nsv5160013mobile element insertion1nstd203human GRCh38 chr14: 31,199,322-31,199,339 , GRCh37.p13 chr14: 31,668,528-31,668,545 HECTD1
    nsv5156726mobile element insertion1nstd203human GRCh38 chr14: 31,142,763-31,142,767 , GRCh37.p13 chr14: 31,611,969-31,611,973 RNU6-541P, HECTD1
    nsv5149956mobile element insertion1nstd203human GRCh38 chr14: 31,133,693-31,133,712 , GRCh37.p13 chr14: 31,602,899-31,602,918 HECTD1
    nsv5149893mobile element insertion1nstd203human GRCh38 chr14: 31,130,725-31,130,737 , GRCh37.p13 chr14: 31,599,931-31,599,943 HECTD1
    nsv5144253mobile element insertion1nstd203human GRCh38 chr14: 31,142,760-31,142,767 , GRCh37.p13 chr14: 31,611,966-31,611,973 HECTD1, RNU6-541P
    nsv5143764mobile element insertion1nstd203human GRCh38 chr14: 31,142,753-31,142,767 , GRCh37.p13 chr14: 31,611,959-31,611,973 HECTD1, RNU6-541P
    nsv4994163copy number variation1nstd200human GRCh38 chr14: 31,207,560-31,233,356 , GRCh37.p13 chr14: 31,676,766-31,702,562 HECTD1
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