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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068649inversion1nstd229human GRCh38 chr19: 4,313,135-7,007,201 , GRCh37.p13 chr19: 4,313,132-7,007,212 CAPS, SH2D3A, 93 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7066921inversion1nstd229human GRCh38 chr19: 4,809,260-7,077,959 , GRCh37.p13 chr19: 4,809,272-7,077,970 MLLT1, GPR108, 74 more genes
    nsv7059289inversion1nstd229human GRCh38 chr19: 5,886,502-5,991,855 , GRCh37.p13 chr19: 5,886,513-5,991,866 RANBP3, NDUFA11, 4 more genes
    nsv7016490copy number variation1nstd229human GRCh38 chr19: 5,647,801-5,918,500 , GRCh37.p13 chr19: 5,647,812-5,918,511 CAPS, LONP1, 16 more genes
    nsv7013846copy number variation1nstd229human GRCh38 chr19: 5,827,692-5,949,398 , GRCh37.p13 chr19: 5,827,703-5,949,409 RANBP3, NDUFA11, 7 more genes
    nsv7001484copy number variation1nstd229human GRCh38 chr19: 5,775,912-5,928,696 , GRCh37.p13 chr19: 5,775,923-5,928,707 NDUFA11, FUT5, 10 more genes
    nsv6599224inversion1nstd223human GRCh38 chr19: 5,796,324-7,362,002 , GRCh37.p13 chr19: 5,796,335-7,426,888 C3, CAPS, 53 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6597141inversion1nstd223human GRCh38 chr19: 5,796,177-7,362,164 , GRCh37.p13 chr19: 5,796,188-7,427,050 MBD3L5, FUT6, 53 more genes
    nsv6529759copy number variation1nstd223human GRCh38 chr19: 5,905,104-5,908,239 , GRCh37.p13 chr19: 5,905,115-5,908,250 VMAC
    nsv6518347copy number variation1nstd223human GRCh38 chr19: 5,519,830-5,914,520 , GRCh37.p13 chr19: 5,519,841-5,914,531 NRTN, VMAC, 19 more genes
    nsv6314807copy number variation1nstd102humanUncertain significance GRCh37 chr19: 5,678,562-5,903,719 , GRCh38.p12 chr19: 5,678,551-5,903,708 VMAC, LOC101928844, 13 more genes
    nsv6310555copy number variation1nstd102humanUncertain significance GRCh37 chr19: 5,894,753-5,903,719 , GRCh38.p12 chr19: 5,894,742-5,903,708 NDUFA11, VMAC
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133468copy number variation1nstd213human GRCh37 chr19: 2,040,000-7,300,001 , GRCh38.p12 chr19: 2,040,001-7,299,990 TLE5, AMH, 192 more genes
    nsv6129185insertion1nstd186human GRCh37 chr19: 5,910,835-5,910,864 , GRCh38.p12 chr19: 5,910,824-5,910,853 VMAC
    nsv6106390insertion1nstd212human GRCh38 chr19: 5,910,824-5,910,824 , GRCh37.p13 chr19: 5,910,835-5,910,835 VMAC
    nsv5978956insertion1nstd209human GRCh38 chr19: 5,910,815-5,910,815 , GRCh37.p13 chr19: 5,910,826-5,910,826 VMAC
    nsv5977090insertion1nstd209human GRCh38 chr19: 5,907,610-5,907,610 , GRCh37.p13 chr19: 5,907,621-5,907,621 VMAC
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