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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148208copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 41,197,867-41,234,371 , GRCh38.p12 chr17: 43,045,850-43,082,354 BRCA1, RPL21P4
    nsv7148199copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 41,249,356-41,275,984 , GRCh38.p12 chr17: 43,097,339-43,123,967 BRCA1, NBR2
    nsv7137004copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 41,223,256-41,267,742 , GRCh38.p12 chr17: 43,071,239-43,115,725 BRCA1, RPL21P4
    nsv7136989copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,199,721-41,277,501 , GRCh38.p12 chr17: 43,047,704-43,125,484 BRCA1, RPL21P4, 1 more genes
    nsv7136947copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,209,153-41,222,944 , GRCh38.p12 chr17: 43,057,136-43,070,927 BRCA1
    nsv7136945copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,203,135-41,277,501 , GRCh38.p12 chr17: 43,051,118-43,125,484 NBR2, RPL21P4, 1 more genes
    nsv7098822delins1nstd102humanPathogenic GRCh37 chr17: 41,193,677-41,198,103 , GRCh38 chr17: 43,041,660-43,046,086 BRCA1
    nsv7098812copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,198,622-41,200,740 , GRCh38 chr17: 43,046,605-43,048,723 BRCA1
    nsv7098800copy number variation1nstd102humanPathogenic GRCh38 chr17: 43,044,922-43,051,619 , GRCh37 chr17: 41,196,939-41,203,636 BRCA1
    nsv7098795copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,248,474-41,255,890 , GRCh38 chr17: 43,096,457-43,103,873 BRCA1
    nsv7098779complex substitution1nstd102humanPathogenic GRCh37 chr17: 41,213,079-41,215,742 , GRCh38.p12 chr17: 43,061,062-43,063,725 BRCA1
    nsv7098767copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,189,424-41,200,475 , GRCh38.p12 chr17: 43,037,407-43,048,458 BRCA1
    nsv7098762copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,230,031-41,253,797 , GRCh38.p12 chr17: 43,078,014-43,101,780 RPL21P4, BRCA1
    nsv7098733copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,254,111-41,264,129 , GRCh38.p12 chr17: 43,102,094-43,112,112 BRCA1
    nsv7098731copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,221,355-41,380,248 , GRCh38.p12 chr17: 43,069,338-43,228,197 BRCA1, NBR1, 7 more genes
    nsv7095340copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 41,245,526-41,252,711 , GRCh38.p12 chr17: 43,093,509-43,100,694 BRCA1
    nsv7095339copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,226,328-41,228,651 , GRCh38.p12 chr17: 43,074,311-43,076,634 BRCA1
    nsv7095338copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,209,048-41,226,558 , GRCh38.p12 chr17: 43,057,031-43,074,541 BRCA1
    nsv7095337copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,196,977-41,199,745 , GRCh38.p12 chr17: 43,044,960-43,047,728 BRCA1
    nsv7095336copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,196,353-41,215,988 , GRCh38.p12 chr17: 43,044,336-43,063,971 BRCA1
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