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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056655inversion1nstd229human GRCh38 chr2: 79,142,296-79,180,181 , GRCh37.p13 chr2: 79,369,422-79,407,307 REG3A
    nsv7056588inversion1nstd229human GRCh38 chr2: 79,151,776-79,155,743 , GRCh37.p13 chr2: 79,378,902-79,382,869 REG3A
    nsv7052000inversion1nstd229human GRCh38 chr2: 79,142,216-79,225,670 , GRCh37.p13 chr2: 79,369,342-79,452,796 REG3A
    nsv7047431inversion1nstd229human GRCh38 chr2: 78,843,494-79,214,096 , GRCh37.p13 chr2: 79,070,620-79,441,222 REG1B, RNU6-812P, 6 more genes
    nsv7043678inversion1nstd229human GRCh38 chr2: 78,909,860-79,766,861 , GRCh37.p13 chr2: 79,136,986-79,993,987 REG1CP, CTNNA2-AS1, 10 more genes
    nsv7039989inversion1nstd229human GRCh38 chr2: 74,303,206-79,264,856 , GRCh37.p13 chr2: 74,530,333-79,491,982 WBP1, DCTN1-AS1, 80 more genes
    nsv6697168copy number variation1nstd229human GRCh38 chr2: 79,153,621-79,157,362 , GRCh37.p13 chr2: 79,380,747-79,384,488 REG3A
    nsv6688958copy number variation1nstd229human GRCh38 chr2: 78,953,066-81,234,791 , GRCh37.p13 chr2: 79,180,192-81,461,915 GNA13P1, LOC105374823, 17 more genes
    nsv6686974copy number variation1nstd229human GRCh38 chr2: 78,195,929-79,340,476 , GRCh37.p13 chr2: 78,423,055-79,567,602 REG1CP, LOC100421651, 13 more genes
    nsv6686066copy number variation1nstd229human GRCh38 chr2: 78,308,222-79,522,493 , GRCh37.p13 chr2: 78,535,348-79,749,619 CTNNA2, CYCSP6, 14 more genes
    nsv6685762copy number variation1nstd229human GRCh38 chr2: 79,129,704-79,217,451 , GRCh37.p13 chr2: 79,356,830-79,444,577 REG1CP, REG3A
    nsv6680926copy number variation1nstd229human GRCh38 chr2: 78,154,785-79,817,747 , GRCh37.p13 chr2: 78,381,911-80,044,873 REG1B, LOC105374820, 18 more genes
    nsv6680879copy number variation1nstd229human GRCh38 chr2: 78,362,714-79,751,963 , GRCh37.p13 chr2: 78,589,840-79,979,089 CTNNA2-AS1, LOC105374820, 17 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628408copy number variation1nstd224human GRCh37 chr2: 78,680,056-79,827,274 , GRCh38.p12 chr2: 78,452,930-79,600,148 CTNNA2, REG1CP, 13 more genes
    nsv6535788inversion1nstd223human GRCh38 chr2: 79,151,770-79,155,743 , GRCh37.p13 chr2: 79,378,896-79,382,869 REG3A
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv5980185inversion1nstd209human GRCh38 chr2: 79,155,478-79,159,172 , GRCh37.p13 chr2: 79,382,604-79,386,298 REG3A
    nsv5975543inversion1nstd209human GRCh38 chr2: 79,026,827-79,158,710 , GRCh37.p13 chr2: 79,253,953-79,385,836 REG3A, REG1A, 3 more genes
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