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Items: 1 to 20 of 565

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145826insertion1nstd232human GRCh37.p13 chr2: 230,636,349-230,636,349 , GRCh38.p12 chr2: 229,771,633-229,771,633 TRIP12
    nsv7057490inversion1nstd229human GRCh38 chr2: 229,854,307-229,857,323 , GRCh37.p13 chr2: 230,719,023-230,722,039 TRIP12
    nsv7055195inversion1nstd229human GRCh38 chr2: 229,914,894-229,914,941 , GRCh37.p13 chr2: 230,779,610-230,779,657 TRIP12
    nsv7054895inversion1nstd229human GRCh38 chr2: 229,787,965-232,576,060 , GRCh37.p13 chr2: 230,652,681-233,440,770 GPR55, RN7SL834P, 80 more genes
    nsv7053498inversion1nstd229human GRCh38 chr2: 229,877,247-229,878,965 , GRCh37.p13 chr2: 230,741,963-230,743,681 TRIP12
    nsv7050091inversion1nstd229human GRCh38 chr2: 229,892,462-229,996,054 , GRCh37.p13 chr2: 230,757,178-230,860,770 FBXO36, LOC105373924, 4 more genes
    nsv7049962inversion1nstd229human GRCh38 chr2: 227,539,172-230,370,061 , GRCh37.p13 chr2: 228,403,888-231,234,776 SPHKAP, TRIP12, 37 more genes
    nsv7048964inversion1nstd229human GRCh38 chr2: 229,716,736-229,865,614 , GRCh37.p13 chr2: 230,581,452-230,730,330 TRIP12
    nsv7046239inversion1nstd229human GRCh38 chr2: 229,826,292-229,956,702 , GRCh37.p13 chr2: 230,691,008-230,821,418 TRIP12, RNU6-964P, 3 more genes
    nsv7045442inversion1nstd229human GRCh38 chr2: 229,826,152-229,925,487 , GRCh37.p13 chr2: 230,690,868-230,790,203 RNU6-613P, TRIP12, 1 more genes
    nsv6697487copy number variation1nstd229human GRCh38 chr2: 229,665,414-229,769,974 , GRCh37.p13 chr2: 230,530,130-230,634,690 DNER, TRIP12
    nsv6696950copy number variation1nstd229human GRCh38 chr2: 229,554,046-229,764,206 , GRCh37.p13 chr2: 230,418,762-230,628,922 LOC105373923, DNER, 2 more genes
    nsv6696864copy number variation1nstd229human GRCh38 chr2: 229,644,090-229,862,763 , GRCh37.p13 chr2: 230,508,806-230,727,479 DNER, TRIP12
    nsv6696659copy number variation1nstd229human GRCh38 chr2: 229,898,545-229,900,646 , GRCh37.p13 chr2: 230,763,261-230,765,362 TRIP12
    nsv6696019copy number variation1nstd229human GRCh38 chr2: 229,872,303-229,878,874 , GRCh37.p13 chr2: 230,737,019-230,743,590 TRIP12
    nsv6696007copy number variation1nstd229human GRCh38 chr2: 229,715,301-229,920,000 , GRCh37.p13 chr2: 230,580,017-230,784,716 TRIP12, RNU6-613P
    nsv6695658copy number variation1nstd229human GRCh38 chr2: 229,765,590-229,769,456 , GRCh37.p13 chr2: 230,630,306-230,634,172 TRIP12
    nsv6691937copy number variation1nstd229human GRCh38 chr2: 229,715,463-229,862,830 , GRCh37.p13 chr2: 230,580,179-230,727,546 TRIP12
    nsv6690921copy number variation1nstd229human GRCh38 chr2: 229,888,601-230,011,100 , GRCh37.p13 chr2: 230,753,317-230,875,816 TRIP12, FBXO36, 4 more genes
    nsv6690695copy number variation1nstd229human GRCh38 chr2: 229,779,291-229,781,108 , GRCh37.p13 chr2: 230,644,007-230,645,824 TRIP12
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