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Items: 1 to 20 of 582

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099244copy number variation1nstd231human GRCh38.p12 chr1: 166,864,890-169,028,321 , GRCh37 chr1: 166,834,127-168,997,559 CD247, DPT, 49 more genes
    nsv7044226inversion1nstd229human GRCh38 chr1: 167,418,610-167,418,631 , GRCh37.p13 chr1: 167,387,847-167,387,868 POU2F1
    nsv7040274inversion1nstd229human GRCh38 chr1: 167,262,830-167,313,055 , GRCh37.p13 chr1: 167,232,067-167,282,292 POU2F1
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6644242copy number variation1nstd229human GRCh38 chr1: 167,345,679-167,354,999 , GRCh37.p13 chr1: 167,314,916-167,324,236 POU2F1
    nsv6644241copy number variation1nstd229human GRCh38 chr1: 167,324,382-167,324,445 , GRCh37.p13 chr1: 167,293,619-167,293,682 POU2F1
    nsv6644240copy number variation1nstd229human GRCh38 chr1: 167,291,223-167,301,410 , GRCh37.p13 chr1: 167,260,460-167,270,647 POU2F1
    nsv6644239copy number variation1nstd229human GRCh38 chr1: 167,270,558-167,699,449 , GRCh37.p13 chr1: 167,239,795-167,668,686 POU2F1, LOC101928512, 6 more genes
    nsv6644184copy number variation1nstd229human GRCh38 chr1: 167,392,871-167,445,339 , GRCh37.p13 chr1: 167,362,108-167,414,576 POU2F1, CD247
    nsv6644182copy number variation1nstd229human GRCh38 chr1: 167,299,050-167,316,195 , GRCh37.p13 chr1: 167,268,287-167,285,432 POU2F1
    nsv6644181copy number variation1nstd229human GRCh38 chr1: 167,239,847-167,322,449 , GRCh37.p13 chr1: 167,209,084-167,291,686 POU2F1
    nsv6644124copy number variation1nstd229human GRCh38 chr1: 167,322,225-167,322,387 , GRCh37.p13 chr1: 167,291,462-167,291,624 POU2F1
    nsv6644123copy number variation1nstd229human GRCh38 chr1: 167,314,232-167,318,707 , GRCh37.p13 chr1: 167,283,469-167,287,944 POU2F1
    nsv6644122copy number variation1nstd229human GRCh38 chr1: 167,310,520-167,313,627 , GRCh37.p13 chr1: 167,279,757-167,282,864 POU2F1
    nsv6644121copy number variation1nstd229human GRCh38 chr1: 167,297,467-167,301,828 , GRCh37.p13 chr1: 167,266,704-167,271,065 POU2F1
    nsv6644120copy number variation1nstd229human GRCh38 chr1: 167,240,823-167,252,036 , GRCh37.p13 chr1: 167,210,060-167,221,273 POU2F1
    nsv6644119copy number variation1nstd229human GRCh38 chr1: 167,239,628-167,242,445 , GRCh37.p13 chr1: 167,208,865-167,211,682 POU2F1
    nsv6644118copy number variation1nstd229human GRCh38 chr1: 167,238,012-167,260,362 , GRCh37.p13 chr1: 167,207,249-167,229,599 POU2F1
    nsv6644016copy number variation1nstd229human GRCh38 chr1: 167,244,390-167,304,722 , GRCh37.p13 chr1: 167,213,627-167,273,959 POU2F1
    nsv6643748copy number variation1nstd229human GRCh38 chr1: 167,274,803-167,281,024 , GRCh37.p13 chr1: 167,244,040-167,250,261 POU2F1
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