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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131463insertion1nstd186human GRCh37 chr16: 4,847,664-4,847,670 , GRCh38.p12 chr16: 4,797,663-4,797,669 ROGDI
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5967652insertion1nstd209human GRCh38 chr16: 4,797,618-4,797,618 , GRCh37.p13 chr16: 4,847,619-4,847,619 ROGDI
    nsv5940740copy number variation1nstd209human GRCh38 chr16: 4,802,683-4,802,832 , GRCh37.p13 chr16: 4,852,684-4,852,833 GLYR1, ROGDI
    nsv5645098insertion1nstd207human GRCh38 chr16: 4,797,618-4,797,618 , GRCh37.p13 chr16: 4,847,619-4,847,619 ROGDI
    nsv5544818insertion1nstd206human GRCh38 chr16: 4,797,663-4,797,669 , GRCh37.p13 chr16: 4,847,664-4,847,670 ROGDI
    nsv5536690insertion1nstd206human GRCh38 chr16: 4,802,944-4,802,958 , GRCh37.p13 chr16: 4,852,945-4,852,959 GLYR1, ROGDI
    nsv5008116copy number variation1nstd200human GRCh38 chr16: 4,732,537-5,127,796 , GRCh37.p13 chr16: 4,782,538-5,177,797 NAGPA, PPL, 16 more genes
    nsv4866538copy number variation1nstd200human GRCh37 chr16: 4,852,684-4,852,825 , GRCh38.p12 chr16: 4,802,683-4,802,824 GLYR1, ROGDI
    nsv4757934insertion1nstd199human GRCh37 chr16: 4,847,630-4,847,630 , GRCh38.p12 chr16: 4,797,629-4,797,629 ROGDI
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4720502insertion1nstd186human GRCh37 chr16: 4,847,619-4,847,619 , GRCh38.p12 chr16: 4,797,618-4,797,618 ROGDI
    nsv4683689copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,777,699-4,852,592 , GRCh38.p12 chr16: 3,727,698-4,802,591 UBALD1, HMOX2, 30 more genes
    nsv4625895copy number variation1nstd183human GRCh37 chr16: 4,828,843-4,905,232 , GRCh38.p12 chr16: 4,778,842-4,855,231 UBN1, ROGDI, 3 more genes
    nsv4624899copy number variation1nstd183human GRCh37 chr16: 4,834,456-4,905,232 , GRCh38.p12 chr16: 4,784,455-4,855,231 GLYR1, SEPTIN12, 3 more genes
    nsv4620304copy number variation1nstd183human GRCh37 chr16: 4,848,114-4,851,800 , GRCh38.p12 chr16: 4,798,113-4,801,799 GLYR1, ROGDI
    nsv4549036insertion1nstd166human GRCh37.p13 chr16: 4,847,619-4,847,619 , GRCh38.p12 chr16: 4,797,618-4,797,618 ROGDI
    nsv4456218copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,731,117-5,325,699 , GRCh38.p12 chr16: 3,681,116-5,275,698 CORO7-PAM16, DBIP3, 46 more genes
    nsv4453988copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,727,698-4,802,591 , GRCh37 chr16: 3,777,699-4,852,592 RN7SL850P, ZNF500, 30 more genes
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