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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923279copy number variation1nstd209human GRCh38 chr8: 27,826,528-27,826,813 , GRCh37.p13 chr8: 27,684,045-27,684,330 PBK
    nsv5915676copy number variation1nstd209human GRCh38 chr8: 27,818,452-27,818,527 , GRCh37.p13 chr8: 27,675,969-27,676,044 PBK
    nsv5694606mobile element insertion1nstd211human GRCh38 chr8: 27,831,603-27,831,603 , GRCh37.p13 chr8: 27,689,120-27,689,120 PBK
    nsv5580322copy number variation1nstd207human GRCh38 chr8: 27,826,528-27,826,813 , GRCh37.p13 chr8: 27,684,045-27,684,330 PBK
    nsv5534129insertion1nstd206human GRCh38 chr8: 27,831,533-27,831,549 , GRCh37.p13 chr8: 27,689,050-27,689,066 PBK
    nsv5480690copy number variation1nstd206human GRCh38 chr8: 27,826,543-27,826,814 , GRCh37.p13 chr8: 27,684,060-27,684,331 PBK
    nsv5394032mobile element insertion1nstd206human GRCh38 chr8: 27,831,603-27,831,654 , GRCh37.p13 chr8: 27,689,120-27,689,171 PBK
    nsv5382938mobile element deletion2nstd186human GRCh37 chr8: 27,684,060-27,684,331 , GRCh38.p12 chr8: 27,826,543-27,826,814 PBK
    nsv5214725mobile element deletion1nstd204human GRCh38.p13 chr8: 27,826,543-27,826,814 , GRCh37.p13 chr8: 27,684,060-27,684,331 PBK
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5196326mobile element insertion1nstd203human GRCh38 chr8: 27,812,624-27,812,641 , GRCh37.p13 chr8: 27,670,141-27,670,158 PBK, ESCO2
    nsv5117316mobile element insertion1nstd203human GRCh38 chr8: 27,831,587-27,831,603 , GRCh37.p13 chr8: 27,689,104-27,689,120 PBK
    nsv5101090mobile element insertion1nstd203human GRCh38 chr8: 27,831,586-27,831,603 , GRCh37.p13 chr8: 27,689,103-27,689,120 PBK
    nsv4893288mobile element deletion1nstd200human GRCh38 chr8: 27,826,543-27,826,814 , GRCh37.p13 chr8: 27,684,060-27,684,331 PBK
    nsv4787441mobile element deletion1nstd200human GRCh37 chr8: 27,684,060-27,684,331 , GRCh38.p12 chr8: 27,826,543-27,826,814 PBK
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4738759copy number variation1nstd199human GRCh37 chr8: 27,684,055-27,684,341 , GRCh38.p12 chr8: 27,826,538-27,826,824 PBK
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4725465insertion1nstd186human GRCh37 chr8: 27,689,050-27,689,050 , GRCh38.p12 chr8: 27,831,533-27,831,533 PBK
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