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Items: 1 to 20 of 979

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147909copy number variation1nstd232human GRCh37.p13 chr7: 78,657,561-78,657,612 , GRCh38.p12 chr7: 79,028,245-79,028,296 MAGI2, RNU6-337P
    nsv7145894insertion1nstd232human GRCh37.p13 chr7: 77,687,320-77,687,320 , GRCh38.p12 chr7: 78,058,003-78,058,003 MAGI2
    nsv7144986copy number variation1nstd232human GRCh37.p13 chr7: 78,953,956-78,954,024 , GRCh38.p12 chr7: 79,324,640-79,324,708 MAGI2
    nsv7144794copy number variation1nstd232human GRCh37.p13 chr7: 78,135,193-78,135,241 , GRCh38.p12 chr7: 78,505,876-78,505,924 MAGI2
    nsv7140113copy number variation1nstd232human GRCh37.p13 chr7: 78,953,844-78,953,896 , GRCh38.p12 chr7: 79,324,528-79,324,580 MAGI2
    nsv7097756copy number variation1nstd102humanUncertain significance GRCh37 chr7: 77,648,632-77,998,550 , GRCh38.p12 chr7: 78,019,315-78,369,233 MAGI2, RPL13AP17
    nsv7097388copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,530,028-79,082,636 , GRCh38.p12 chr7: 77,900,711-79,453,320 MAGI2-AS3, LOC100421387, 9 more genes
    nsv7055029inversion1nstd229human GRCh38 chr7: 78,854,292-78,870,193 , GRCh37.p13 chr7: 78,483,608-78,499,509 MAGI2
    nsv7054110inversion1nstd229human GRCh38 chr7: 79,272,805-79,277,304 , GRCh37.p13 chr7: 78,902,121-78,906,620 MAGI2
    nsv7053247inversion1nstd229human GRCh38 chr7: 78,214,845-78,230,039 , GRCh37.p13 chr7: 77,844,162-77,859,356 MAGI2
    nsv7050017inversion1nstd229human GRCh38 chr7: 78,863,435-78,873,798 , GRCh37.p13 chr7: 78,492,751-78,503,114 MAGI2
    nsv7048114inversion1nstd229human GRCh38 chr7: 76,979,006-85,395,330 , GRCh37.p13 chr7: 76,608,323-85,024,646 LOC100420647, LOC105375369, 77 more genes
    nsv7047505inversion1nstd229human GRCh38 chr7: 79,355,776-79,355,831 , GRCh37.p13 chr7: 78,985,092-78,985,147 MAGI2
    nsv7042753inversion1nstd229human GRCh38 chr7: 78,081,882-78,081,994 , GRCh37.p13 chr7: 77,711,199-77,711,311 MAGI2
    nsv7040760inversion1nstd229human GRCh38 chr7: 78,755,794-78,782,604 , GRCh37.p13 chr7: 78,385,110-78,411,920 MAGI2
    nsv7038722inversion1nstd229human GRCh38 chr7: 78,854,498-78,854,513 , GRCh37.p13 chr7: 78,483,814-78,483,829 MAGI2
    nsv7038325inversion1nstd229human GRCh38 chr7: 78,495,690-78,495,756 , GRCh37.p13 chr7: 78,125,007-78,125,073 MAGI2
    nsv6838029copy number variation1nstd229human GRCh38 chr7: 78,693,458-78,697,604 , GRCh37.p13 chr7: 78,322,774-78,326,920 MAGI2
    nsv6837989copy number variation1nstd229human GRCh38 chr7: 78,059,225-78,059,449 , GRCh37.p13 chr7: 77,688,542-77,688,766 MAGI2
    nsv6837816copy number variation1nstd229human GRCh38 chr7: 78,737,966-78,739,858 , GRCh37.p13 chr7: 78,367,282-78,369,174 MAGI2
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