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Items: 1 to 20 of 328

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955451insertion1nstd209human GRCh38 chr2: 119,510,701-119,510,701 , GRCh37.p13 chr2: 120,268,277-120,268,277 SCTR
    nsv5899084copy number variation1nstd209human GRCh38 chr2: 119,502,973-119,503,657 , GRCh37.p13 chr2: 120,260,549-120,261,233 SCTR
    nsv5898250copy number variation1nstd209human GRCh38 chr2: 119,444,536-119,445,000 , GRCh37.p13 chr2: 120,202,112-120,202,576 SCTR
    nsv5891212copy number variation1nstd209human GRCh38 chr2: 119,510,709-119,510,915 , GRCh37.p13 chr2: 120,268,285-120,268,491 SCTR
    nsv5831121copy number variation1nstd209human GRCh38 chr2: 119,407,244-119,444,066 , GRCh37.p13 chr2: 120,164,820-120,201,642 TMEM37, SCTR
    nsv5693366mobile element insertion1nstd211human GRCh38 chr2: 119,440,759-119,440,759 , GRCh37.p13 chr2: 120,198,335-120,198,335 SCTR
    nsv5690873mobile element insertion2nstd211human GRCh38 chr2: 119,510,709-119,510,709 , GRCh37.p13 chr2: 120,268,285-120,268,285 SCTR
    nsv5677405mobile element insertion1nstd211human GRCh38 chr2: 119,467,853-119,467,853 , GRCh37.p13 chr2: 120,225,429-120,225,429 SCTR
    nsv5622568insertion1nstd207human GRCh38 chr2: 119,510,698-119,510,698 , GRCh37.p13 chr2: 120,268,274-120,268,274 SCTR
    nsv5621863insertion1nstd207human GRCh38 chr2: 119,444,506-119,444,506 , GRCh37.p13 chr2: 120,202,082-120,202,082 SCTR
    nsv5621108insertion1nstd207human GRCh38 chr2: 119,444,926-119,444,926 , GRCh37.p13 chr2: 120,202,502-120,202,502 SCTR
    nsv5618379insertion1nstd207human GRCh38 chr2: 119,512,435-119,512,435 , GRCh37.p13 chr2: 120,270,011-120,270,011 SCTR
    nsv5609722insertion1nstd207human GRCh38 chr2: 119,444,880-119,444,880 , GRCh37.p13 chr2: 120,202,456-120,202,456 SCTR
    nsv5579873copy number variation1nstd207human GRCh38 chr2: 119,444,800-119,444,925 , GRCh37.p13 chr2: 120,202,376-120,202,501 SCTR
    nsv5571051copy number variation1nstd207human GRCh38 chr2: 119,444,852-119,444,925 , GRCh37.p13 chr2: 120,202,428-120,202,501 SCTR
    nsv5567673copy number variation1nstd207human GRCh38 chr2: 119,444,381-119,444,740 , GRCh37.p13 chr2: 120,201,957-120,202,316 SCTR
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5551193insertion1nstd206human GRCh38 chr2: 119,510,709-119,510,749 , GRCh37.p13 chr2: 120,268,285-120,268,325 SCTR
    nsv5549875insertion1nstd206human GRCh38 chr2: 119,444,230-119,444,255 , GRCh37.p13 chr2: 120,201,806-120,201,831 SCTR
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