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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6714894copy number variation1nstd229human GRCh38 chr3: 14,064,301-14,499,300 , GRCh37.p13 chr3: 14,105,801-14,540,808 TMEM43, SLC6A6, 11 more genes
    nsv6712102copy number variation1nstd229human GRCh38 chr3: 14,119,427-14,119,496 , GRCh37.p13 chr3: 14,160,927-14,160,996 CHCHD4
    nsv6701112copy number variation1nstd229human GRCh38 chr3: 12,689,301-14,136,700 , GRCh37.p13 chr3: 12,730,800-14,178,200 SNORA93, LOC105376957, 28 more genes
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6541743inversion1nstd223human GRCh38 chr3: 14,115,358-14,116,590 , GRCh37.p13 chr3: 14,156,858-14,158,090 CHCHD4
    nsv6538655inversion1nstd223human GRCh38 chr3: 14,115,509-14,116,702 , GRCh37.p13 chr3: 14,157,009-14,158,202 CHCHD4
    nsv6365415copy number variation1nstd223human GRCh38 chr3: 14,119,422-14,119,496 , GRCh37.p13 chr3: 14,160,922-14,160,996 CHCHD4
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    nsv6311955copy number variation1nstd102humanUncertain significance GRCh37 chr3: 14,166,694-14,183,295 , GRCh38.p12 chr3: 14,125,194-14,141,795 CHCHD4, TMEM43
    nsv6165069copy number variation1nstd214human GRCh38 chr3: 14,119,422-14,119,495 , GRCh37.p13 chr3: 14,160,922-14,160,995 CHCHD4
    nsv5991402copy number variation1nstd212human GRCh38 chr3: 14,119,422-14,119,496 , GRCh37.p13 chr3: 14,160,922-14,160,996 CHCHD4
    nsv5904743copy number variation1nstd209human GRCh38 chr3: 14,119,422-14,119,495 , GRCh37.p13 chr3: 14,160,922-14,160,995 CHCHD4
    nsv5673474copy number variation1nstd102humanPathogenic GRCh37 chr3: 14,166,684-14,220,439 , GRCh38.p12 chr3: 14,125,184-14,178,939 XPC, TMEM43, 3 more genes
    nsv5613809insertion1nstd207human GRCh38 chr3: 14,115,358-14,115,358 , GRCh37.p13 chr3: 14,156,858-14,156,858 CHCHD4
    nsv5582439copy number variation1nstd207human GRCh38 chr3: 14,119,422-14,119,495 , GRCh37.p13 chr3: 14,160,922-14,160,995 CHCHD4
    nsv5554106sequence alteration1nstd206human GRCh38 chr3: 14,115,357-14,116,590 , GRCh37.p13 chr3: 14,156,857-14,158,090 CHCHD4
    nsv5543238insertion1nstd206human GRCh38 chr3: 14,115,358-14,115,358 , GRCh37.p13 chr3: 14,156,858-14,156,858 CHCHD4
    nsv5445249copy number variation1nstd206human GRCh38 chr3: 14,119,427-14,119,496 , GRCh37.p13 chr3: 14,160,927-14,160,996 CHCHD4
    nsv5388027copy number variation2nstd186human GRCh37 chr3: 14,160,927-14,160,996 , GRCh38.p12 chr3: 14,119,427-14,119,496 CHCHD4
    nsv5329378translocation1nstd204human GRCh38.p13 chr3: 14,115,363-14,115,363 , GRCh38.p13 chr3: 14,116,460-14,116,460 , GRCh37.p13 chr3: 14,156,863-14,156,863 , GRCh37.p13 chr3: 14,157,960-14,157,960 CHCHD4
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