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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094547copy number variation1nstd102humanPathogenic GRCh37 chr15: 62,146,656-64,747,263 , GRCh38.p12 chr15: 61,854,457-64,455,064 C2CD4A, SNX22, 40 more genes
    nsv7062496inversion1nstd229human GRCh38 chr15: 63,394,953-63,395,013 , GRCh37.p13 chr15: 63,687,152-63,687,212 LINC02568
    nsv6976238copy number variation1nstd229human GRCh38 chr15: 63,420,954-63,427,894 , GRCh37.p13 chr15: 63,713,153-63,720,093 LINC02568
    nsv6969608copy number variation1nstd229human GRCh38 chr15: 63,411,453-63,569,728 , GRCh37.p13 chr15: 63,703,652-63,861,927 LINC02568, USP3
    nsv6969146copy number variation1nstd229human GRCh38 chr15: 63,434,830-63,437,608 , GRCh37.p13 chr15: 63,727,029-63,729,807 LINC02568
    nsv6968211copy number variation1nstd229human GRCh38 chr15: 63,399,501-63,407,300 , GRCh37.p13 chr15: 63,691,700-63,699,499 LINC02568
    nsv6967261copy number variation1nstd229human GRCh38 chr15: 63,400,295-63,402,395 , GRCh37.p13 chr15: 63,692,494-63,694,594 LINC02568
    nsv6965597copy number variation1nstd229human GRCh38 chr15: 63,422,546-63,426,668 , GRCh37.p13 chr15: 63,714,745-63,718,867 LINC02568
    nsv6963579copy number variation1nstd229human GRCh38 chr15: 63,222,593-63,443,339 , GRCh37.p13 chr15: 63,514,792-63,735,538 RAB8B, APH1B, 2 more genes
    nsv6962903copy number variation1nstd229human GRCh38 chr15: 63,419,155-63,427,597 , GRCh37.p13 chr15: 63,711,354-63,719,796 LINC02568
    nsv6960684copy number variation1nstd229human GRCh38 chr15: 62,287,754-63,705,691 , GRCh37.p13 chr15: 62,579,953-63,997,890 MIR8067, RPS27L, 21 more genes
    nsv6960212copy number variation1nstd229human GRCh38 chr15: 63,245,676-63,441,189 , GRCh37.p13 chr15: 63,537,875-63,733,388 RAB8B, APH1B, 2 more genes
    nsv6582043inversion1nstd223human GRCh38 chr15: 63,424,286-63,424,356 , GRCh37.p13 chr15: 63,716,485-63,716,555 LINC02568
    nsv6508363copy number variation1nstd223human GRCh38 chr15: 63,416,871-63,417,329 , GRCh37.p13 chr15: 63,709,070-63,709,528 LINC02568
    nsv6506934copy number variation1nstd223human GRCh38 chr15: 63,423,748-63,425,101 , GRCh37.p13 chr15: 63,715,947-63,717,300 LINC02568
    nsv6504620copy number variation1nstd223human GRCh38 chr15: 63,422,546-63,426,664 , GRCh37.p13 chr15: 63,714,745-63,718,863 LINC02568
    nsv6496928copy number variation1nstd223human GRCh38 chr15: 63,411,453-63,569,726 , GRCh37.p13 chr15: 63,703,652-63,861,925 USP3, LINC02568
    nsv6249752mobile element insertion1nstd215human GRCh38 chr15: 63,408,212-63,408,212 , GRCh37.p13 chr15: 63,700,411-63,700,411 LINC02568
    nsv6203254copy number variation1nstd214human GRCh38 chr15: 63,397,213-63,397,279 , GRCh37.p13 chr15: 63,689,412-63,689,478 LINC02568
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
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