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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096704copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,802,697-172,835,521 , GRCh38.p12 chr3: 169,084,909-173,117,731 GHSR, KLF7P1, 67 more genes
    nsv7057325inversion1nstd229human GRCh38 chr3: 170,134,629-173,143,661 , GRCh37.p13 chr3: 169,852,417-172,861,451 LINC02068, LOC107986052, 45 more genes
    nsv7045710inversion1nstd229human GRCh38 chr3: 172,750,313-172,756,538 , GRCh37.p13 chr3: 172,468,103-172,474,328 ECT2
    nsv6733639copy number variation1nstd229human GRCh38 chr3: 172,751,997-172,754,872 , GRCh37.p13 chr3: 172,469,787-172,472,662 ECT2
    nsv6732747copy number variation1nstd229human GRCh38 chr3: 172,793,817-172,801,467 , GRCh37.p13 chr3: 172,511,607-172,519,257 RNU4-4P, ECT2
    nsv6728012copy number variation1nstd229human GRCh38 chr3: 172,789,314-172,789,554 , GRCh37.p13 chr3: 172,507,104-172,507,344 ECT2
    nsv6725908copy number variation1nstd229human GRCh38 chr3: 172,803,701-172,808,400 , GRCh37.p13 chr3: 172,521,491-172,526,190 ECT2
    nsv6725667copy number variation1nstd229human GRCh38 chr3: 172,745,984-172,756,415 , GRCh37.p13 chr3: 172,463,774-172,474,205 ECT2
    nsv6725561copy number variation1nstd229human GRCh38 chr3: 172,817,968-172,902,911 , GRCh37.p13 chr3: 172,535,758-172,620,701 LOC107986052, SPATA16, 2 more genes
    nsv6721605copy number variation1nstd229human GRCh38 chr3: 172,803,953-172,808,663 , GRCh37.p13 chr3: 172,521,743-172,526,453 ECT2
    nsv6721206copy number variation1nstd229human GRCh38 chr3: 172,672,998-172,759,318 , GRCh37.p13 chr3: 172,390,788-172,477,108 RNU6-547P, NCEH1, 2 more genes
    nsv6720534copy number variation1nstd229human GRCh38 chr3: 172,775,166-172,775,998 , GRCh37.p13 chr3: 172,492,956-172,493,788 ECT2
    nsv6718286copy number variation1nstd229human GRCh38 chr3: 172,775,090-172,775,911 , GRCh37.p13 chr3: 172,492,880-172,493,701 ECT2
    nsv6636531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 172,266,023-172,500,533 , GRCh38.p12 chr3: 172,548,233-172,782,743 LINC02068, RNU6-547P, 4 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6572839inversion1nstd223human GRCh38 chr3: 172,788,967-172,789,398 , GRCh37.p13 chr3: 172,506,757-172,507,188 ECT2
    nsv6572778inversion1nstd223human GRCh38 chr3: 172,767,336-172,767,936 , GRCh37.p13 chr3: 172,485,126-172,485,726 ECT2
    nsv6569844inversion1nstd223human GRCh38 chr3: 172,767,470-172,767,533 , GRCh37.p13 chr3: 172,485,260-172,485,323 ECT2
    nsv6562934inversion1nstd223human GRCh38 chr3: 172,794,840-172,795,197 , GRCh37.p13 chr3: 172,512,630-172,512,987 RNU4-4P, ECT2
    nsv6370828copy number variation1nstd223human GRCh38 chr3: 172,819,801-172,824,400 , GRCh37.p13 chr3: 172,537,591-172,542,190 ECT2
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