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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7042773inversion1nstd229human GRCh38 chr6: 8,542,608-11,835,677 , GRCh37.p13 chr6: 8,542,841-11,835,910 LOC112267952, RNU1-64P, 51 more genes
    nsv6795962copy number variation1nstd229human GRCh38 chr6: 10,200,015-10,372,078 , GRCh37.p13 chr6: 10,200,248-10,372,311 RPL7L1P20, LOC105374920, 4 more genes
    nsv6784012copy number variation1nstd229human GRCh38 chr6: 9,546,200-10,465,508 , GRCh37.p13 chr6: 9,546,433-10,465,741 TFAP2A-AS2, MIR5689HG, 16 more genes
    nsv6783375copy number variation1nstd229human GRCh38 chr6: 10,210,292-10,214,406 , GRCh37.p13 chr6: 10,210,525-10,214,639 OFCC1, RPL21P62
    nsv6409723copy number variation1nstd223human GRCh38 chr6: 7,366,072-12,459,745 , GRCh37.p13 chr6: 7,366,305-12,459,977 EEF1E1, RPS26P29, 82 more genes
    nsv6256641mobile element insertion1nstd215human GRCh38 chr6: 10,214,028-10,214,028 , GRCh37.p13 chr6: 10,214,261-10,214,261 RPL21P62
    nsv6136505copy number variation1nstd213human GRCh37 chr6: 380,000-11,010,001 , GRCh38.p12 chr6: 380,000-11,009,768 BMP6, BPHL, 178 more genes
    nsv6135513copy number variation1nstd213human GRCh37 chr6: 380,000-10,980,001 , GRCh38.p12 chr6: 380,000-10,979,768 BMP6, BPHL, 178 more genes
    nsv5896105copy number variation1nstd209human GRCh38 chr6: 7,548,083-10,446,730 , GRCh37.p13 chr6: 7,548,316-10,446,963 , TFAP2A-AS2, 37 more genes
    nsv5891942copy number variation1nstd209human GRCh38 chr6: 10,214,590-10,214,640 , GRCh37.p13 chr6: 10,214,823-10,214,873 RPL21P62
    nsv5362779translocation1nstd200human GRCh38 chr6: 10,216,689-10,216,689 , GRCh38 chr6: 10,212,917-10,212,917 , GRCh37.p13 chr6: 10,213,150-10,213,150 , GRCh37.p13 chr6: 10,216,922-10,216,922 RPL21P62
    nsv5343013translocation1nstd200human GRCh37 chr6: 10,213,150-10,213,150 , GRCh37 chr6: 10,216,922-10,216,922 , GRCh38.p12 chr6: 10,216,689-10,216,689 , GRCh38.p12 chr6: 10,212,917-10,212,917 RPL21P62
    nsv5331451translocation1nstd200human GRCh37 chr6: 10,214,824-10,214,824 , GRCh37 chr6: 10,214,874-10,214,874 , GRCh38.p12 chr6: 10,214,641-10,214,641 , GRCh38.p12 chr6: 10,214,591-10,214,591 RPL21P62
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 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
    nsv4129448copy number variation1nstd166human GRCh37.p13 chr6: 10,214,824-10,214,874 , GRCh38.p12 chr6: 10,214,591-10,214,641 RPL21P62
    nsv4129110copy number variation1nstd166human GRCh37.p13 chr6: 10,207,781-10,213,150 , GRCh38.p12 chr6: 10,207,548-10,212,917 OFCC1, RPL21P62
    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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