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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131452insertion1nstd186human GRCh37 chr20: 26,186,428-26,186,428 , GRCh38.p12 chr20: 26,205,792-26,205,792 MIR663AHG
    nsv5979798insertion1nstd209human GRCh38 chr20: 26,194,834-26,194,834 , GRCh37.p13 chr20: 26,175,470-26,175,470 MIR663AHG
    nsv5971356insertion1nstd209human GRCh38 chr20: 26,205,782-26,205,782 , GRCh37.p13 chr20: 26,186,418-26,186,418 MIR663AHG
    nsv5966732copy number variation1nstd209human GRCh38 chr20: 26,190,951-26,191,234 , GRCh37.p13 chr20: 26,171,587-26,171,870 MIR663AHG
    nsv5955838copy number variation1nstd209human GRCh38 chr20: 25,923,975-30,219,168 , GRCh37.p13 chr20: 25,904,611-29,453,844 CDC27P3, LOC105379477, 30 more genes
    nsv5948418copy number variation1nstd209human GRCh38 chr20: 26,205,932-26,285,099 , GRCh37.p13 chr20: 26,186,568-26,265,735 MIR663AHG, MIR663A
    nsv5884158copy number variation2nstd209human GRCh38 chr20: 26,206,004-26,208,086 , GRCh37.p13 chr20: 26,186,640-26,188,722 MIR663A, MIR663AHG
    nsv5884004copy number variation1nstd209human GRCh38 chr20: 26,186,664-26,190,228 , GRCh37.p13 chr20: 26,167,300-26,170,864 MIR663AHG
    nsv5882769copy number variation1nstd209human GRCh38 chr20: 26,201,339-26,207,886 , GRCh37.p13 chr20: 26,181,975-26,188,522 MIR663AHG, MIR663A
    nsv5875230copy number variation2nstd209human GRCh38 chr20: 26,208,587-26,219,340 , GRCh37.p13 chr20: 26,189,223-26,199,976 MIR663A, MIR663AHG
    nsv5870184copy number variation1nstd209human GRCh38 chr20: 26,182,887-26,187,463 , GRCh37.p13 chr20: 26,163,523-26,168,099 MIR663AHG
    nsv5703813mobile element insertion1nstd211human GRCh38 chr20: 26,201,774-26,201,774 , GRCh37.p13 chr20: 26,182,410-26,182,410 MIR663AHG
    nsv5666488insertion1nstd207human GRCh38 chr20: 26,205,782-26,205,782 , GRCh37.p13 chr20: 26,186,418-26,186,418 MIR663AHG
    nsv5542403insertion1nstd206human GRCh38 chr20: 26,205,792-26,205,792 , GRCh37.p13 chr20: 26,186,428-26,186,428 MIR663AHG
    nsv5173657mobile element insertion1nstd203human GRCh38 chr20: 26,194,834-26,194,834 , GRCh37.p13 chr20: 26,175,470-26,175,470 MIR663AHG
    nsv5025250copy number variation1nstd200human GRCh38 chr20: 25,920,604-30,215,914 , GRCh37.p13 chr20: 25,901,240-29,450,590 DUX4L37, FRG1EP, 30 more genes
    nsv5021871copy number variation1nstd200human GRCh38 chr20: 26,207,171-26,207,898 , GRCh37.p13 chr20: 26,187,807-26,188,534 MIR663A, MIR663AHG
    nsv5021870copy number variation1nstd200human GRCh38 chr20: 26,191,970-26,197,373 , GRCh37.p13 chr20: 26,172,606-26,178,009 MIR663AHG
    nsv4862424copy number variation1nstd200human GRCh37 chr20: 26,187,807-26,188,534 , GRCh38.p12 chr20: 26,207,171-26,207,898 MIR663AHG, MIR663A
    nsv4755039insertion1nstd199human GRCh37 chr20: 26,186,406-26,186,406 , GRCh38.p12 chr20: 26,205,770-26,205,770 MIR663AHG
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