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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923746copy number variation1nstd209human GRCh38 chr8: 85,440,645-85,440,700 , GRCh37.p13 chr8: 86,352,874-86,352,929 CA3-AS1, CA3
    nsv5708204mobile element insertion2nstd211human GRCh38 chr8: 85,447,165-85,447,165 , GRCh37.p13 chr8: 86,359,394-86,359,394 CA3-AS1, CA3
    nsv5631709insertion1nstd207human GRCh38 chr8: 85,447,149-85,447,149 , GRCh37.p13 chr8: 86,359,378-86,359,378 CA3, CA3-AS1
    nsv5400506mobile element insertion1nstd206human GRCh38 chr8: 85,447,165-85,447,216 , GRCh37.p13 chr8: 86,359,394-86,359,445 CA3-AS1, CA3
    nsv5336263translocation1nstd200human GRCh37 chr8: 86,352,930-86,352,930 , GRCh37 chr8: 86,352,878-86,352,878 , GRCh38.p12 chr8: 85,440,701-85,440,701 , GRCh38.p12 chr8: 85,440,649-85,440,649 CA3-AS1, CA3
    nsv5111168mobile element insertion1nstd203human GRCh38 chr8: 85,447,153-85,447,165 , GRCh37.p13 chr8: 86,359,382-86,359,394 CA3-AS1, CA3
    nsv5106851mobile element insertion1nstd203human GRCh38 chr8: 85,447,156-85,447,163 , GRCh37.p13 chr8: 86,359,385-86,359,392 CA3-AS1, CA3
    nsv5106506mobile element insertion1nstd203human GRCh38 chr8: 85,447,149-85,447,165 , GRCh37.p13 chr8: 86,359,378-86,359,394 CA3, CA3-AS1
    nsv5105273mobile element insertion1nstd203human GRCh38 chr8: 85,447,154-85,447,165 , GRCh37.p13 chr8: 86,359,383-86,359,394 CA3, CA3-AS1
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv5034498inversion1nstd200human GRCh38 chr8: 85,226,325-85,583,275 , GRCh37.p13 chr8: 86,138,554-86,495,504 , CA1, 6 more genes
    nsv4726698insertion1nstd186human GRCh37 chr8: 86,359,378-86,359,378 , GRCh38.p12 chr8: 85,447,149-85,447,149 CA3-AS1, CA3
    nsv4690100mobile element insertion1nstd186human GRCh37 chr8: 86,359,394-86,359,394 , GRCh38.p12 chr8: 85,447,165-85,447,165 CA3, CA3-AS1
    nsv4675773copy number variation1nstd102humanUncertain significance GRCh37 chr8: 85,635,587-86,553,130 , GRCh38.p12 chr8: 84,723,352-85,640,901 CA3, LRRCC1, 16 more genes
    nsv4546643insertion1nstd166human GRCh37.p13 chr8: 86,359,378-86,359,378 , GRCh38.p12 chr8: 85,447,149-85,447,149 CA3-AS1, CA3
    nsv4457216copy number variation1nstd102humanUncertain significance GRCh37 chr8: 84,358,585-89,159,915 , GRCh38.p12 chr8: 83,446,350-88,147,686 LOC100422614, LOC105375933, 61 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456198copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,358,419-86,494,259 , GRCh38.p12 chr8: 85,446,190-85,582,030 CA3, CA3-AS1, 2 more genes
    nsv4456185copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,346,299-86,836,910 , GRCh38.p12 chr8: 85,434,070-85,824,681 REXO1L9P, LOC101929627, 14 more genes
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