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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925447copy number variation1nstd209human GRCh38 chr8: 90,069,895-90,076,277 , GRCh37.p13 chr8: 91,082,123-91,088,505 CALB1
    nsv5909210copy number variation1nstd209human GRCh38 chr8: 90,056,945-90,057,266 , GRCh37.p13 chr8: 91,069,173-91,069,494 CALB1
    nsv5565508copy number variation1nstd207human GRCh38 chr8: 90,056,945-90,057,266 , GRCh37.p13 chr8: 91,069,173-91,069,494 CALB1
    nsv5486582copy number variation1nstd206human GRCh38 chr8: 90,056,956-90,057,267 , GRCh37.p13 chr8: 91,069,184-91,069,495 CALB1
    nsv5384348mobile element deletion2nstd186human GRCh37 chr8: 91,069,184-91,069,495 , GRCh38.p12 chr8: 90,056,956-90,057,267 CALB1
    nsv5247211copy number variation1nstd204human GRCh38.p13 chr8: 90,061,501-90,068,300 , GRCh37.p13 chr8: 91,073,729-91,080,528 CALB1
    nsv5218649mobile element deletion1nstd204human GRCh38.p13 chr8: 90,056,956-90,057,267 , GRCh37.p13 chr8: 91,069,184-91,069,495 CALB1
    nsv5103831mobile element insertion1nstd203human GRCh38 chr8: 90,078,192-90,078,202 , GRCh37.p13 chr8: 91,090,420-91,090,430 CALB1
    nsv5102915mobile element insertion1nstd203human GRCh38 chr8: 90,056,560-90,056,619 , GRCh37.p13 chr8: 91,068,788-91,068,847 CALB1
    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
    nsv4893336mobile element deletion1nstd200human GRCh38 chr8: 90,056,956-90,057,267 , GRCh37.p13 chr8: 91,069,184-91,069,495 CALB1
    nsv4822400copy number variation1nstd200human GRCh37 chr8: 91,082,122-91,088,506 , GRCh38.p12 chr8: 90,069,894-90,076,278 CALB1
    nsv4787506mobile element deletion1nstd200human GRCh37 chr8: 91,069,184-91,069,495 , GRCh38.p12 chr8: 90,056,956-90,057,267 CALB1
    nsv4749737copy number variation1nstd199human GRCh37 chr8: 91,069,179-91,069,501 , GRCh38.p12 chr8: 90,056,951-90,057,273 CALB1
    nsv4729552copy number variation1nstd102humanUncertain significance GRCh37 chr8: 88,194,550-91,779,543 , GRCh38.p12 chr8: 87,182,322-90,767,315 RIPK2, RNU6-925P, 29 more genes
    nsv4707311copy number variation4nstd195human GRCh37 chr8: 91,069,173-91,069,174 , GRCh38.p12 chr8: 90,056,945-90,056,946 CALB1
    nsv4675461copy number variation1nstd102humanUncertain significance GRCh37 chr8: 90,758,337-91,556,317 , GRCh38.p12 chr8: 89,746,109-90,544,089 OSGIN2, RNU6-925P, 9 more genes
    nsv4651656mobile element deletion1nstd186human GRCh37 chr8: 91,069,174-91,069,495 , GRCh38.p12 chr8: 90,056,946-90,057,267 CALB1
    nsv4648666copy number variation1nstd186human GRCh37 chr8: 91,069,184-91,069,495 , GRCh38.p12 chr8: 90,056,956-90,057,267 CALB1
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