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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142602copy number variation1nstd232human GRCh37.p13 chr14: 39,746,884-39,746,951 , GRCh38.p12 chr14: 39,277,680-39,277,747 MIA2
    nsv7138115copy number variation1nstd232human GRCh37.p13 chr14: 39,746,893-39,746,979 , GRCh38.p12 chr14: 39,277,689-39,277,775 MIA2
    nsv7073626inversion1nstd229human GRCh38 chr14: 39,255,773-39,305,161 , GRCh37.p13 chr14: 39,724,977-39,774,365 MIA2-AS1, MIA2
    nsv7065540inversion1nstd229human GRCh38 chr14: 39,270,500-39,279,992 , GRCh37.p13 chr14: 39,739,704-39,749,196 MIA2
    nsv6957181copy number variation1nstd229human GRCh38 chr14: 39,170,101-39,246,700 , GRCh37.p13 chr14: 39,639,305-39,715,904 MIA2, LOC100313942, 3 more genes
    nsv6955475copy number variation1nstd229human GRCh38 chr14: 39,269,701-39,320,000 , GRCh37.p13 chr14: 39,738,905-39,789,204 MIA2
    nsv6955460copy number variation1nstd229human GRCh38 chr14: 39,287,126-39,294,251 , GRCh37.p13 chr14: 39,756,330-39,763,455 MIA2
    nsv6954879copy number variation1nstd229human GRCh38 chr14: 39,332,960-39,343,980 , GRCh37.p13 chr14: 39,802,164-39,813,184 MIA2
    nsv6954853copy number variation1nstd229human GRCh38 chr14: 39,255,229-39,259,880 , GRCh37.p13 chr14: 39,724,433-39,729,084 MIA2
    nsv6953358copy number variation1nstd229human GRCh38 chr14: 39,333,661-39,337,037 , GRCh37.p13 chr14: 39,802,865-39,806,241 MIA2
    nsv6952503copy number variation1nstd229human GRCh38 chr14: 39,240,948-39,253,640 , GRCh37.p13 chr14: 39,710,152-39,722,844 MIA2
    nsv6948517copy number variation1nstd229human GRCh38 chr14: 39,311,325-39,311,367 , GRCh37.p13 chr14: 39,780,529-39,780,571 MIA2
    nsv6945235copy number variation1nstd229human GRCh38 chr14: 39,264,063-39,264,818 , GRCh37.p13 chr14: 39,733,267-39,734,022 MIA2-AS1, MIA2
    nsv6944795copy number variation1nstd229human GRCh38 chr14: 39,291,849-39,347,885 , GRCh37.p13 chr14: 39,761,053-39,817,089 MIA2
    nsv6944686copy number variation1nstd229human GRCh38 chr14: 39,327,601-39,330,900 , GRCh37.p13 chr14: 39,796,805-39,800,104 MIA2
    nsv6944433copy number variation1nstd229human GRCh38 chr14: 39,281,159-39,297,804 , GRCh37.p13 chr14: 39,750,363-39,767,008 MIA2
    nsv6944028copy number variation1nstd229human GRCh38 chr14: 39,379,524-39,383,311 , GRCh37.p13 chr14: 39,848,728-39,852,515 MIA2, COILP1
    nsv6943340copy number variation1nstd229human GRCh38 chr14: 39,229,601-39,257,500 , GRCh37.p13 chr14: 39,698,805-39,726,704 MIA2
    nsv6943317copy number variation1nstd229human GRCh38 chr14: 39,331,844-39,335,576 , GRCh37.p13 chr14: 39,801,048-39,804,780 MIA2
    nsv6942415copy number variation1nstd229human GRCh38 chr14: 39,372,928-39,375,150 , GRCh37.p13 chr14: 39,842,132-39,844,354 MIA2
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