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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7043314inversion1nstd229human GRCh38 chr2: 79,131,305-79,134,781 , GRCh37.p13 chr2: 79,358,431-79,361,907 REG1CP
    nsv7039989inversion1nstd229human GRCh38 chr2: 74,303,206-79,264,856 , GRCh37.p13 chr2: 74,530,333-79,491,982 WBP1, DCTN1-AS1, 80 more genes
    nsv7039844inversion1nstd229human GRCh38 chr2: 79,130,937-79,137,901 , GRCh37.p13 chr2: 79,358,063-79,365,027 REG1CP
    nsv6695622copy number variation1nstd229human GRCh38 chr2: 79,133,937-79,136,291 , GRCh37.p13 chr2: 79,361,063-79,363,417 REG1CP
    nsv6693934copy number variation1nstd229human GRCh38 chr2: 79,129,301-79,136,000 , GRCh37.p13 chr2: 79,356,427-79,363,126 REG1CP
    nsv6693611copy number variation1nstd229human GRCh38 chr2: 79,134,841-79,148,688 , GRCh37.p13 chr2: 79,361,967-79,375,814 REG1CP
    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
    nsv6353978copy number variation1nstd223human GRCh38 chr2: 79,134,801-79,137,900 , GRCh37.p13 chr2: 79,361,927-79,365,026 REG1CP
    nsv6343518copy number variation1nstd223human GRCh38 chr2: 79,129,256-79,135,957 , GRCh37.p13 chr2: 79,356,382-79,363,083 REG1CP
    nsv6341428copy number variation1nstd223human GRCh38 chr2: 79,138,207-79,138,845 , GRCh37.p13 chr2: 79,365,333-79,365,971 REG1CP
    nsv6335899copy number variation1nstd223human GRCh38 chr2: 79,134,841-79,148,687 , GRCh37.p13 chr2: 79,361,967-79,375,813 REG1CP
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