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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137075copy number variation1nstd102humanUncertain significance GRCh38 chr15: 44,330,225-44,821,972 , GRCh37.p13 chr15: 44,622,423-45,114,170 PATL2, CTDSPL2, 10 more genes
    nsv7137026copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,865,019-44,876,011 , GRCh38.p12 chr15: 44,572,821-44,583,813 SPG11
    nsv7094710copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,941,044-44,944,484 , GRCh38.p12 chr15: 44,648,846-44,652,286 SPG11
    nsv7094709copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,855,319-44,952,834 , GRCh38.p12 chr15: 44,563,121-44,660,636 EIF3J, SPG11
    nsv7094537copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,912,368-44,925,855 , GRCh38.p12 chr15: 44,620,170-44,633,657 SPG11
    nsv7094536copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-44,878,413 , GRCh38.p12 chr15: 44,563,121-44,586,215 EIF3J, SPG11
    nsv7094521copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 44,876,757-44,884,528 , GRCh38.p12 chr15: 44,584,559-44,592,330 SPG11
    nsv7094374copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,884,509-44,884,656 , GRCh38.p12 chr15: 44,592,311-44,592,458 SPG11
    nsv7094292copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,877,814-44,955,845 , GRCh38.p12 chr15: 44,585,616-44,663,647 SPG11
    nsv7094291copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,877,814-44,878,413 , GRCh38.p12 chr15: 44,585,616-44,586,215 SPG11
    nsv7093617insertion1nstd102humanPathogenic GRCh37 chr15: 44,864,897-44,864,897 , GRCh38 chr15: 44,572,699-44,572,699 SPG11
    nsv7093494delins1nstd102humanPathogenic GRCh37 chr15: 44,887,634-44,887,639 , GRCh38 chr15: 44,595,436-44,595,441 SPG11
    nsv7093056copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,861,704-44,876,011 , GRCh38.p12 chr15: 44,569,506-44,583,813 SPG11
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6974572copy number variation1nstd229human GRCh38 chr15: 44,558,850-44,587,420 , GRCh37.p13 chr15: 44,851,048-44,879,618 EIF3J, SPG11
    nsv6973688copy number variation1nstd229human GRCh38 chr15: 44,636,256-44,640,324 , GRCh37.p13 chr15: 44,928,454-44,932,522 SPG11
    nsv6966426copy number variation1nstd229human GRCh38 chr15: 44,569,997-44,578,321 , GRCh37.p13 chr15: 44,862,195-44,870,519 SPG11
    nsv6965669copy number variation1nstd229human GRCh38 chr15: 44,663,464-44,672,156 , GRCh37.p13 chr15: 44,955,662-44,964,354 PATL2, SPG11
    nsv6962143copy number variation1nstd229human GRCh38 chr15: 44,632,663-44,664,382 , GRCh37.p13 chr15: 44,924,861-44,956,580 PATL2, SPG11
    nsv6962115copy number variation1nstd229human GRCh38 chr15: 44,585,316-44,591,723 , GRCh37.p13 chr15: 44,877,514-44,883,921 SPG11
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