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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6697270copy number variation1nstd229human GRCh38 chr2: 176,304,199-176,308,247 , GRCh37.p13 chr2: 177,168,927-177,172,975 MTX2
    nsv6695923copy number variation1nstd229human GRCh38 chr2: 176,203,210-176,289,410 , GRCh37.p13 chr2: 177,067,938-177,154,138 RPSAP25, MTX2
    nsv6695028copy number variation1nstd229human GRCh38 chr2: 176,331,906-176,334,613 , GRCh37.p13 chr2: 177,196,634-177,199,341 MTX2
    nsv6686305copy number variation1nstd229human GRCh38 chr2: 176,252,501-176,275,600 , GRCh37.p13 chr2: 177,117,229-177,140,328 MTX2
    nsv6684966copy number variation1nstd229human GRCh38 chr2: 176,306,701-176,311,200 , GRCh37.p13 chr2: 177,171,429-177,175,928 MTX2
    nsv6683988copy number variation1nstd229human GRCh38 chr2: 176,309,248-176,309,299 , GRCh37.p13 chr2: 177,173,976-177,174,027 MTX2
    nsv6678942copy number variation1nstd229human GRCh38 chr2: 176,261,470-176,394,677 , GRCh37.p13 chr2: 177,126,198-177,259,405 PPIAP67, MTX2
    nsv6637115copy number variation1nstd102humanPathogenic GRCh37 chr2: 175,143,352-180,999,636 , GRCh38.p12 chr2: 174,278,624-180,134,909 RNU6-5P, LOC101927073, 107 more genes
    nsv6550749inversion1nstd223human GRCh38 chr2: 176,312,705-176,313,586 , GRCh37.p13 chr2: 177,177,433-177,178,314 MTX2
    nsv6354143copy number variation1nstd223human GRCh38 chr2: 176,326,339-176,327,026 , GRCh37.p13 chr2: 177,191,067-177,191,754 MTX2
    nsv6353445copy number variation1nstd223human GRCh38 chr2: 176,300,699-176,301,153 , GRCh37.p13 chr2: 177,165,427-177,165,881 MTX2
    nsv6353258copy number variation1nstd223human GRCh38 chr2: 176,203,210-176,289,410 , GRCh37.p13 chr2: 177,067,938-177,154,138 MTX2, RPSAP25
    nsv6351783copy number variation1nstd223human GRCh38 chr2: 176,284,194-176,285,795 , GRCh37.p13 chr2: 177,148,922-177,150,523 MTX2
    nsv6350689copy number variation1nstd223human GRCh38 chr2: 176,330,901-176,331,700 , GRCh37.p13 chr2: 177,195,629-177,196,428 MTX2
    nsv6348712copy number variation1nstd223human GRCh38 chr2: 176,293,269-176,295,822 , GRCh37.p13 chr2: 177,157,997-177,160,550 MTX2
    nsv6345996copy number variation1nstd223human GRCh38 chr2: 176,335,901-176,336,800 , GRCh37.p13 chr2: 177,200,629-177,201,528 MTX2, PPIAP67
    nsv6345548copy number variation1nstd223human GRCh38 chr2: 176,290,701-176,292,700 , GRCh37.p13 chr2: 177,155,429-177,157,428 MTX2
    nsv6343137copy number variation1nstd223human GRCh38 chr2: 176,303,001-176,304,200 , GRCh37.p13 chr2: 177,167,729-177,168,928 MTX2
    nsv6339290copy number variation1nstd223human GRCh38 chr2: 176,288,801-176,289,900 , GRCh37.p13 chr2: 177,153,529-177,154,628 MTX2
    nsv6336874copy number variation1nstd223human GRCh38 chr2: 176,331,906-176,334,608 , GRCh37.p13 chr2: 177,196,634-177,199,336 MTX2
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