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Items: 1 to 20 of 367

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055193inversion1nstd229human GRCh38 chr2: 119,610,070-119,674,944 , GRCh37.p13 chr2: 120,367,646-120,432,520 CFAP221
    nsv7050777inversion1nstd229human GRCh38 chr2: 117,420,323-122,585,255 , GRCh37.p13 chr2: 118,177,899-123,342,831 LOC105373578, RPL17P15, 65 more genes
    nsv7044064inversion1nstd229human GRCh38 chr2: 112,019,946-120,004,832 , GRCh37.p13 chr2: 112,777,523-120,762,408 LOC105373563, IL1A, 112 more genes
    nsv6695137copy number variation1nstd229human GRCh38 chr2: 119,595,241-119,601,093 , GRCh37.p13 chr2: 120,352,817-120,358,669 CFAP221
    nsv6692997copy number variation1nstd229human GRCh38 chr2: 119,589,026-119,589,228 , GRCh37.p13 chr2: 120,346,602-120,346,804 CFAP221
    nsv6692426copy number variation1nstd229human GRCh38 chr2: 119,582,857-119,586,758 , GRCh37.p13 chr2: 120,340,433-120,344,334 CFAP221
    nsv6692425copy number variation1nstd229human GRCh38 chr2: 119,575,412-119,577,019 , GRCh37.p13 chr2: 120,332,988-120,334,595 CFAP221
    nsv6691726copy number variation1nstd229human GRCh38 chr2: 119,624,022-119,642,210 , GRCh37.p13 chr2: 120,381,598-120,399,786 CFAP221
    nsv6690452copy number variation1nstd229human GRCh38 chr2: 119,545,332-119,566,717 , GRCh37.p13 chr2: 120,302,908-120,324,293 CFAP221
    nsv6689192copy number variation1nstd229human GRCh38 chr2: 119,605,715-120,065,324 , GRCh37.p13 chr2: 120,363,291-120,822,900 EPB41L5, PTPN4, 6 more genes
    nsv6686383copy number variation1nstd229human GRCh38 chr2: 119,634,763-119,653,195 , GRCh37.p13 chr2: 120,392,339-120,410,771 CFAP221
    nsv6681551copy number variation1nstd229human GRCh38 chr2: 119,555,333-119,557,023 , GRCh37.p13 chr2: 120,312,909-120,314,599 CFAP221
    nsv6680914copy number variation1nstd229human GRCh38 chr2: 119,639,401-119,643,800 , GRCh37.p13 chr2: 120,396,977-120,401,376 CFAP221
    nsv6680536copy number variation1nstd229human GRCh38 chr2: 119,549,567-119,556,592 , GRCh37.p13 chr2: 120,307,143-120,314,168 CFAP221
    nsv6680388copy number variation1nstd229human GRCh38 chr2: 119,610,101-119,662,000 , GRCh37.p13 chr2: 120,367,677-120,419,576 CFAP221
    nsv6679459copy number variation1nstd229human GRCh38 chr2: 119,311,516-119,861,317 , GRCh37.p13 chr2: 120,069,092-120,618,893 RPL17P15, TMEM177, 8 more genes
    nsv6678337copy number variation1nstd229human GRCh38 chr2: 119,592,601-119,681,700 , GRCh37.p13 chr2: 120,350,177-120,439,276 CFAP221, TMEM177
    nsv6678310copy number variation1nstd229human GRCh38 chr2: 119,639,008-119,656,419 , GRCh37.p13 chr2: 120,396,584-120,413,995 CFAP221
    nsv6678188copy number variation1nstd229human GRCh38 chr2: 119,551,901-119,556,500 , GRCh37.p13 chr2: 120,309,477-120,314,076 CFAP221
    nsv6636976copy number variation1nstd102humanUncertain significance GRCh37 chr2: 120,079,538-120,626,557 , GRCh38.p12 chr2: 119,321,962-119,868,981 TMEM177, RPL17P15, 8 more genes
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