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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6976352copy number variation1nstd229human GRCh38 chr14: 74,313,916-74,316,496 , GRCh37.p13 chr14: 74,780,619-74,783,199 VRTN
    nsv6975445copy number variation1nstd229human GRCh38 chr14: 74,306,419-74,312,903 , GRCh37.p13 chr14: 74,773,122-74,779,606 VRTN, SUB1P2
    nsv6966487copy number variation1nstd229human GRCh38 chr14: 74,340,600-74,343,968 , GRCh37.p13 chr14: 74,807,303-74,810,671 VRTN
    nsv6965540copy number variation1nstd229human GRCh38 chr14: 74,305,501-74,307,300 , GRCh37.p13 chr14: 74,772,204-74,774,003 VRTN, SUB1P2
    nsv6961036copy number variation1nstd229human GRCh38 chr14: 74,322,706-74,326,127 , GRCh37.p13 chr14: 74,789,409-74,792,830 VRTN
    nsv6958982copy number variation1nstd229human GRCh38 chr14: 74,298,906-74,303,505 , GRCh37.p13 chr14: 74,765,609-74,770,208 VRTN, ABCD4, 1 more genes
    nsv6634490copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 74,764,773-74,769,768 , GRCh38.p12 chr14: 74,298,070-74,303,065 ABCD4, VRTN
    nsv6595030inversion1nstd223human GRCh38 chr14: 74,329,122-74,329,783 , GRCh37.p13 chr14: 74,795,825-74,796,486 VRTN
    nsv6592514inversion1nstd223human GRCh38 chr14: 74,321,656-74,324,229 , GRCh37.p13 chr14: 74,788,359-74,790,932 VRTN
    nsv6591288inversion1nstd223human GRCh38 chr14: 74,332,524-74,333,373 , GRCh37.p13 chr14: 74,799,227-74,800,076 VRTN
    nsv6587426inversion1nstd223human GRCh38 chr14: 74,335,974-74,336,365 , GRCh37.p13 chr14: 74,802,677-74,803,068 VRTN
    nsv6495168copy number variation1nstd223human GRCh38 chr14: 74,298,906-74,303,501 , GRCh37.p13 chr14: 74,765,609-74,770,204 ABCD4, VRTN, 1 more genes
    nsv6493625copy number variation1nstd223human GRCh38 chr14: 74,333,639-74,335,135 , GRCh37.p13 chr14: 74,800,342-74,801,838 VRTN
    nsv6491139copy number variation1nstd223human GRCh38 chr14: 74,340,106-74,341,520 , GRCh37.p13 chr14: 74,806,809-74,808,223 VRTN
    nsv6490752copy number variation1nstd223human GRCh38 chr14: 74,305,465-74,307,270 , GRCh37.p13 chr14: 74,772,168-74,773,973 VRTN, SUB1P2
    nsv6489103copy number variation1nstd223human GRCh38 chr14: 74,330,524-74,341,531 , GRCh37.p13 chr14: 74,797,227-74,808,234 VRTN
    nsv6485934copy number variation1nstd223human GRCh38 chr14: 74,312,006-74,312,977 , GRCh37.p13 chr14: 74,778,709-74,779,680 VRTN
    nsv6482369copy number variation1nstd223human GRCh38 chr14: 74,329,101-74,331,700 , GRCh37.p13 chr14: 74,795,804-74,798,403 VRTN
    nsv6477298copy number variation1nstd223human GRCh38 chr14: 74,345,663-74,346,043 , GRCh37.p13 chr14: 74,812,366-74,812,746 VRTN
    nsv6476640copy number variation1nstd223human GRCh38 chr14: 74,333,294-74,333,711 , GRCh37.p13 chr14: 74,799,997-74,800,414 VRTN
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