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Items: 1 to 20 of 519

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057524inversion1nstd229human GRCh38 chr3: 16,508,371-16,508,451 , GRCh37.p13 chr3: 16,549,878-16,549,958 RFTN1
    nsv7049810inversion1nstd229human GRCh38 chr3: 16,139,271-16,577,361 , GRCh37.p13 chr3: 16,180,778-16,618,868 OXNAD1, LINC00690, 5 more genes
    nsv7042364inversion1nstd229human GRCh38 chr3: 16,500,429-16,500,486 , GRCh37.p13 chr3: 16,541,936-16,541,993 RFTN1
    nsv6716888copy number variation1nstd229human GRCh38 chr3: 16,076,014-16,572,211 , GRCh37.p13 chr3: 16,117,521-16,613,718 OXNAD1, LOC107986065, 5 more genes
    nsv6714113copy number variation1nstd229human GRCh38 chr3: 16,318,257-16,321,294 , GRCh37.p13 chr3: 16,359,764-16,362,801 RFTN1, OXNAD1
    nsv6713729copy number variation1nstd229human GRCh38 chr3: 16,329,679-16,336,725 , GRCh37.p13 chr3: 16,371,186-16,378,232 RFTN1, OXNAD1
    nsv6713146copy number variation1nstd229human GRCh38 chr3: 16,338,031-16,338,096 , GRCh37.p13 chr3: 16,379,538-16,379,603 OXNAD1, RFTN1
    nsv6713100copy number variation1nstd229human GRCh38 chr3: 15,359,925-17,364,956 , GRCh37.p13 chr3: 15,401,432-17,406,448 RNU6-1024P, COLQ, 27 more genes
    nsv6713016copy number variation1nstd229human GRCh38 chr3: 16,314,722-16,317,205 , GRCh37.p13 chr3: 16,356,229-16,358,712 OXNAD1, RFTN1
    nsv6712172copy number variation1nstd229human GRCh38 chr3: 16,315,472-16,315,509 , GRCh37.p13 chr3: 16,356,979-16,357,016 RFTN1, OXNAD1
    nsv6711904copy number variation1nstd229human GRCh38 chr3: 16,437,128-16,440,661 , GRCh37.p13 chr3: 16,478,635-16,482,168 RFTN1
    nsv6711235copy number variation1nstd229human GRCh38 chr3: 16,439,049-16,485,198 , GRCh37.p13 chr3: 16,480,556-16,526,705 RFTN1
    nsv6709594copy number variation1nstd229human GRCh38 chr3: 16,508,870-16,525,544 , GRCh37.p13 chr3: 16,550,377-16,567,051 RFTN1
    nsv6707828copy number variation1nstd229human GRCh38 chr3: 16,366,195-16,366,233 , GRCh37.p13 chr3: 16,407,702-16,407,740 OXNAD1, RFTN1
    nsv6707740copy number variation1nstd229human GRCh38 chr3: 16,332,401-16,339,100 , GRCh37.p13 chr3: 16,373,908-16,380,607 OXNAD1, RFTN1
    nsv6707668copy number variation1nstd229human GRCh38 chr3: 16,514,096-16,524,079 , GRCh37.p13 chr3: 16,555,603-16,565,586 RFTN1
    nsv6707436copy number variation1nstd229human GRCh38 chr3: 16,318,439-16,323,233 , GRCh37.p13 chr3: 16,359,946-16,364,740 OXNAD1, RFTN1
    nsv6707382copy number variation1nstd229human GRCh38 chr3: 16,434,101-16,438,600 , GRCh37.p13 chr3: 16,475,608-16,480,107 RFTN1
    nsv6706523copy number variation1nstd229human GRCh38 chr3: 16,357,982-16,366,261 , GRCh37.p13 chr3: 16,399,489-16,407,768 RFTN1, OXNAD1
    nsv6706489copy number variation1nstd229human GRCh38 chr3: 16,348,978-16,349,068 , GRCh37.p13 chr3: 16,390,485-16,390,575 OXNAD1, RFTN1
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