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Items: 1 to 20 of 549

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954622insertion1nstd209human GRCh38 chr9: 91,798,642-91,798,642 , GRCh37.p13 chr9: 94,560,924-94,560,924 ROR2
    nsv5951828insertion1nstd209human GRCh38 chr9: 91,798,381-91,798,381 , GRCh37.p13 chr9: 94,560,663-94,560,663 ROR2
    nsv5926881copy number variation1nstd209human GRCh38 chr9: 91,796,742-91,797,144 , GRCh37.p13 chr9: 94,559,024-94,559,426 ROR2
    nsv5922581copy number variation1nstd209human GRCh38 chr9: 91,796,743-91,796,984 , GRCh37.p13 chr9: 94,559,025-94,559,266 ROR2
    nsv5921334copy number variation1nstd209human GRCh38 chr9: 91,866,156-91,866,453 , GRCh37.p13 chr9: 94,628,438-94,628,735 , ROR2
    nsv5919046copy number variation1nstd209human GRCh38 chr9: 91,776,706-91,777,664 , GRCh37.p13 chr9: 94,538,988-94,539,946 ROR2
    nsv5918680copy number variation1nstd209human GRCh38 chr9: 91,868,146-91,869,412 , GRCh37.p13 chr9: 94,630,428-94,631,694 , ROR2
    nsv5917325copy number variation1nstd209human GRCh38 chr9: 91,727,045-91,727,170 , GRCh37.p13 chr9: 94,489,327-94,489,452 ROR2
    nsv5917176copy number variation1nstd209human GRCh38 chr9: 91,882,824-91,882,950 , GRCh37.p13 chr9: 94,645,106-94,645,232 , ROR2
    nsv5917137copy number variation1nstd209human GRCh38 chr9: 91,734,437-91,734,590 , GRCh37.p13 chr9: 94,496,719-94,496,872 ROR2
    nsv5916816copy number variation1nstd209human GRCh38 chr9: 91,823,340-91,823,494 , GRCh37.p13 chr9: 94,585,622-94,585,776 ROR2
    nsv5911990copy number variation1nstd209human GRCh38 chr9: 91,870,089-91,870,155 , GRCh37.p13 chr9: 94,632,371-94,632,437 , ROR2
    nsv5911094copy number variation1nstd209human GRCh38 chr9: 91,749,803-91,749,997 , GRCh37.p13 chr9: 94,512,085-94,512,279 ROR2
    nsv5909869copy number variation1nstd209human GRCh38 chr9: 91,796,758-91,796,865 , GRCh37.p13 chr9: 94,559,040-94,559,147 ROR2
    nsv5862851copy number variation1nstd209human GRCh38 chr9: 91,868,178-91,869,377 , GRCh37.p13 chr9: 94,630,460-94,631,659 , ROR2
    nsv5698607mobile element insertion1nstd211human GRCh38 chr9: 91,868,363-91,868,363 , GRCh37.p13 chr9: 94,630,645-94,630,645 , ROR2
    nsv5697897mobile element insertion1nstd211human GRCh38 chr9: 91,781,418-91,781,418 , GRCh37.p13 chr9: 94,543,700-94,543,700 ROR2
    nsv5695214mobile element insertion2nstd211human GRCh38 chr9: 91,926,726-91,926,726 , GRCh37.p13 chr9: 94,689,008-94,689,008 ROR2
    nsv5673830copy number variation1nstd102humanPathogenic GRCh37 chr9: 94,485,944-94,538,110 , GRCh38.p12 chr9: 91,723,662-91,775,828 ROR2
    nsv5638637insertion1nstd207human GRCh38 chr9: 91,754,782-91,754,782 , GRCh37.p13 chr9: 94,517,064-94,517,064 ROR2
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