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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5726132mobile element insertion1nstd211human GRCh38 chr6: 16,134,940-16,134,940 , GRCh37.p13 chr6: 16,135,171-16,135,171 MYLIP
    nsv5564204copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr6: 15,523,206-16,146,982 , GRCh38.p12 chr6: 15,522,975-16,146,751 MDH1P2, LINC02543, 8 more genes
    nsv5557247mobile element insertion1nstd206human GRCh38 chr6: 16,134,940-16,134,991 , GRCh37.p13 chr6: 16,135,171-16,135,222 MYLIP
    nsv5179720mobile element insertion1nstd203human GRCh38 chr6: 16,134,926-16,134,940 , GRCh37.p13 chr6: 16,135,157-16,135,171 MYLIP
    nsv5080686mobile element insertion1nstd203human GRCh38 chr6: 16,134,940-16,134,953 , GRCh37.p13 chr6: 16,135,171-16,135,184 MYLIP
    nsv4934455copy number variation1nstd200human GRCh38 chr6: 16,129,960-16,292,983 , GRCh37.p13 chr6: 16,130,191-16,293,214 MIR4639, GMPR, 5 more genes
    nsv4932862copy number variation1nstd200human GRCh38 chr6: 16,120,263-16,128,324 , GRCh37.p13 chr6: 16,120,494-16,128,555 MYLIP
    nsv4828515copy number variation1nstd200human GRCh37 chr6: 16,130,191-16,293,214 , GRCh38.p12 chr6: 16,129,960-16,292,983 MRPL42P2, MYLIP, 5 more genes
    nsv4568628mobile element insertion1nstd166human GRCh37.p13 chr6: 16,135,157-16,135,157 , GRCh38.p12 chr6: 16,134,926-16,134,926 MYLIP
    nsv4545192insertion1nstd166human GRCh37.p13 chr6: 16,137,391-16,137,391 , GRCh38.p12 chr6: 16,137,160-16,137,160 MYLIP
    nsv4457139copy number variation1nstd102humanUncertain significance GRCh37 chr6: 14,715,955-17,223,929 , GRCh38.p12 chr6: 14,715,724-17,223,698 MDH1P2, ATXN1, 28 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4456299copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,910,125-22,000,204 , GRCh38.p12 chr6: 13,909,894-21,999,975 LOC101928354, MBOAT1, 101 more genes
    nsv4455888copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,248,587-18,083,552 , GRCh38.p12 chr6: 13,248,355-18,083,321 RNU6-522P, LOC105374942, 70 more genes
    nsv4131070copy number variation1nstd166human GRCh37.p13 chr6: 16,149,715-16,149,912 , GRCh38.p12 chr6: 16,149,484-16,149,681 MYLIP
    nsv4123280copy number variation1nstd166human GRCh37.p13 chr6: 16,127,000-16,132,000 , GRCh38.p12 chr6: 16,126,769-16,131,769 MYLIP
    nsv4120844copy number variation1nstd166human GRCh37.p13 chr6: 16,151,659-16,151,735 , GRCh38.p12 chr6: 16,151,428-16,151,504 MYLIP
    nsv3922594copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,311,751-16,295,791 , GRCh38 chr6: 13,311,519-16,295,560 , NCBI36 chr6: 13,419,730-16,403,770 LOC107986571, LOC105374947, 47 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
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