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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898786copy number variation1nstd209human GRCh38 chr4: 122,663,837-122,663,888 , GRCh37.p13 chr4: 123,584,992-123,585,043 IL21-AS1
    nsv5722206mobile element insertion1nstd211human GRCh38 chr4: 122,634,752-122,634,752 , GRCh37.p13 chr4: 123,555,907-123,555,907 IL21-AS1
    nsv5686299mobile element insertion2nstd211human GRCh38 chr4: 122,623,239-122,623,239 , GRCh37.p13 chr4: 123,544,394-123,544,394 IL21-AS1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5465847copy number variation1nstd206human GRCh38 chr4: 122,642,174-122,643,338 , GRCh37.p13 chr4: 123,563,329-123,564,493 IL21-AS1
    nsv5396697mobile element insertion1nstd206human GRCh38 chr4: 122,623,239-122,623,290 , GRCh37.p13 chr4: 123,544,394-123,544,445 IL21-AS1
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5347080translocation1nstd200human GRCh38 chr4: 122,619,178-122,619,178 , GRCh38 chr4: 122,618,337-122,618,337 , GRCh37.p13 chr4: 123,539,492-123,539,492 , GRCh37.p13 chr4: 123,540,333-123,540,333 IL21-AS1, IL21
    nsv5307139copy number variation1nstd204human GRCh38.p13 chr4: 122,630,019-122,634,529 , GRCh37.p13 chr4: 123,551,174-123,555,684 IL21-AS1
    nsv5237256copy number variation1nstd204human GRCh38.p13 chr4: 122,630,001-122,634,500 , GRCh37.p13 chr4: 123,551,156-123,555,655 IL21-AS1
    nsv5224111copy number variation1nstd204human GRCh38.p13 chr4: 122,629,780-122,634,604 , GRCh37.p13 chr4: 123,550,935-123,555,759 IL21-AS1
    nsv5094286mobile element insertion1nstd203human GRCh38 chr4: 122,667,211-122,667,225 , GRCh37.p13 chr4: 123,588,366-123,588,380 IL21-AS1
    nsv5091206mobile element insertion1nstd203human GRCh38 chr4: 122,649,337-122,649,358 , GRCh37.p13 chr4: 123,570,492-123,570,513 IL21-AS1
    nsv4935648copy number variation1nstd200human GRCh38 chr4: 122,673,852-122,675,225 , GRCh37.p13 chr4: 123,595,007-123,596,380 IL21-AS1
    nsv4935647copy number variation1nstd200human GRCh38 chr4: 122,659,409-122,660,426 , GRCh37.p13 chr4: 123,580,564-123,581,581 IL21-AS1
    nsv4935646copy number variation1nstd200human GRCh38 chr4: 122,642,174-122,643,338 , GRCh37.p13 chr4: 123,563,329-123,564,493 IL21-AS1
    nsv4935645copy number variation1nstd200human GRCh38 chr4: 122,630,024-122,634,525 , GRCh37.p13 chr4: 123,551,179-123,555,680 IL21-AS1
    nsv4808268copy number variation1nstd200human GRCh37 chr4: 123,595,007-123,596,380 , GRCh38.p12 chr4: 122,673,852-122,675,225 IL21-AS1
    nsv4808267copy number variation1nstd200human GRCh37 chr4: 123,563,329-123,564,493 , GRCh38.p12 chr4: 122,642,174-122,643,338 IL21-AS1
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