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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972000insertion1nstd209human GRCh38 chr11: 77,832,984-77,832,984 , GRCh37.p13 chr11: 77,544,030-77,544,030 AAMDC, RSF1
    nsv5912040copy number variation1nstd209human GRCh38 chr11: 77,896,906-77,897,614 , GRCh37.p13 chr11: 77,607,952-77,608,660 AAMDC, INTS4
    nsv5720331mobile element insertion1nstd211human GRCh38 chr11: 77,870,677-77,870,677 , GRCh37.p13 chr11: 77,581,723-77,581,723 AAMDC, RSF1
    nsv5700751mobile element insertion1nstd211human GRCh38 chr11: 77,855,737-77,855,737 , GRCh37.p13 chr11: 77,566,783-77,566,783 RSF1, AAMDC
    nsv5695852mobile element insertion1nstd211human GRCh38 chr11: 77,873,083-77,873,083 , GRCh37.p13 chr11: 77,584,129-77,584,129 INTS4, AAMDC
    nsv5591034copy number variation1nstd207human GRCh38 chr11: 77,896,921-77,897,630 , GRCh37.p13 chr11: 77,607,967-77,608,676 AAMDC, INTS4
    nsv5538767insertion1nstd206human GRCh38 chr11: 77,824,853-77,824,904 , GRCh37.p13 chr11: 77,535,899-77,535,950 AAMDC, RSF1
    nsv5509206copy number variation1nstd206human GRCh38 chr11: 77,896,901-77,897,654 , GRCh37.p13 chr11: 77,607,947-77,608,700 INTS4, AAMDC
    nsv5505031copy number variation1nstd206human GRCh38 chr11: 77,898,997-77,899,604 , GRCh37.p13 chr11: 77,610,043-77,610,650 INTS4, AAMDC
    nsv5504208copy number variation1nstd206human GRCh38 chr11: 77,832,540-77,833,208 , GRCh37.p13 chr11: 77,543,586-77,544,254 RSF1, AAMDC
    nsv5498619copy number variation1nstd206human GRCh38 chr11: 77,823,629-77,824,304 , GRCh37.p13 chr11: 77,534,675-77,535,350 RSF1, AAMDC
    nsv5394686mobile element insertion1nstd206human GRCh38 chr11: 77,873,083-77,873,134 , GRCh37.p13 chr11: 77,584,129-77,584,180 INTS4, AAMDC
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5355394translocation1nstd200human GRCh38 chr11: 77,896,906-77,896,906 , GRCh38 chr11: 77,897,634-77,897,634 , GRCh37.p13 chr11: 77,607,952-77,607,952 , GRCh37.p13 chr11: 77,608,680-77,608,680 INTS4, AAMDC
    nsv5338929translocation1nstd200human GRCh37 chr11: 77,588,530-77,588,530 , GRCh37 chr11: 77,588,286-77,588,286 , GRCh38.p12 chr11: 77,877,484-77,877,484 , GRCh38.p12 chr11: 77,877,240-77,877,240 AAMDC, INTS4
    nsv5330439translocation1nstd200human GRCh37 chr11: 77,608,680-77,608,680 , GRCh37 chr11: 77,607,952-77,607,952 , GRCh38.p12 chr11: 77,896,906-77,896,906 , GRCh38.p12 chr11: 77,897,634-77,897,634 INTS4, AAMDC
    nsv5302607copy number variation1nstd204human GRCh37.p13 chr11: 77,607,942-77,608,697 , GRCh38.p13 chr11: 77,896,896-77,897,651 AAMDC, INTS4
    nsv4989068copy number variation1nstd200human GRCh38 chr11: 77,881,989-77,900,300 , GRCh37.p13 chr11: 77,593,035-77,611,346 INTS4, AAMDC
    nsv4989067copy number variation1nstd200human GRCh38 chr11: 77,839,766-78,289,807 , GRCh37.p13 chr11: 77,550,812-78,000,853 KCTD21-AS1, NDUFC2, 13 more genes
    nsv4989066copy number variation1nstd200human GRCh38 chr11: 77,814,098-77,827,051 , GRCh37.p13 chr11: 77,525,144-77,538,097 RSF1, AAMDC, 1 more genes
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