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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097620copy number variation1nstd102humanUncertain significance GRCh37 chr7: 2,577,703-2,972,240 , GRCh38.p12 chr7: 2,538,069-2,932,606 LOC107986760, TTYH3, 6 more genes
    nsv7057091inversion1nstd229human GRCh38 chr7: 2,273,784-2,696,327 , GRCh37.p13 chr7: 2,313,419-2,735,961 BRAT1, NGRNP3, 13 more genes
    nsv7055142inversion1nstd229human GRCh38 chr7: 2,588,325-2,801,871 , GRCh37.p13 chr7: 2,627,959-2,841,505 IQCE, LOC107986760, 3 more genes
    nsv7052786inversion1nstd229human GRCh38 chr7: 2,451,109-6,490,439 , GRCh37.p13 chr7: 2,490,744-6,530,070 LOC105375130, DAGLB, 72 more genes
    nsv6817892copy number variation1nstd229human GRCh38 chr7: 2,591,694-2,709,380 , GRCh37.p13 chr7: 2,631,328-2,749,014 LOC107986760, AMZ1, 2 more genes
    nsv6815941copy number variation1nstd229human GRCh38 chr7: 2,646,938-2,651,771 , GRCh37.p13 chr7: 2,686,572-2,691,405 TTYH3
    nsv6815704copy number variation1nstd229human GRCh38 chr7: 2,256,868-2,660,330 , GRCh37.p13 chr7: 2,296,503-2,699,964 NGRNP3, IMMP1LP3, 13 more genes
    nsv6809502copy number variation1nstd229human GRCh38 chr7: 2,642,501-2,645,200 , GRCh37.p13 chr7: 2,682,135-2,684,834 TTYH3
    nsv6808763copy number variation1nstd229human GRCh38 chr7: 2,361,837-2,647,130 , GRCh37.p13 chr7: 2,401,472-2,686,764 KIF19BP, TTYH3, 10 more genes
    nsv6808514copy number variation1nstd229human GRCh38 chr7: 2,556,929-2,763,850 , GRCh37.p13 chr7: 2,596,563-2,803,484 TTYH3, GNA12, 3 more genes
    nsv6806241copy number variation1nstd229human GRCh38 chr7: 2,642,542-2,645,267 , GRCh37.p13 chr7: 2,682,176-2,684,901 TTYH3
    nsv6804373copy number variation1nstd229human GRCh38 chr7: 2,618,301-2,647,300 , GRCh37.p13 chr7: 2,657,935-2,686,934 TTYH3, LOC107986760
    nsv6801350copy number variation1nstd229human GRCh38 chr7: 2,585,640-2,672,230 , GRCh37.p13 chr7: 2,625,274-2,711,864 IQCE, TTYH3, 1 more genes
    nsv6635870copy number variation2nstd227human GRCh37 chr7: 2,669,587-2,686,059 , GRCh38.p12 chr7: 2,629,953-2,646,425 TTYH3
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634339copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-9,649,794 , GRCh38.p12 chr7: 43,360-9,610,164 MRM2, FOXL3, 182 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631630copy number variation1nstd224human GRCh37 chr7: 2,703,464-2,747,902 , GRCh38.p12 chr7: 2,663,830-2,708,268 TTYH3, AMZ1
    nsv6614407copy number variation1nstd223human GRCh38 chr7: 2,642,215-2,646,827 , GRCh37.p13 chr7: 2,681,849-2,686,461 TTYH3
    nsv6607612copy number variation1nstd223human GRCh38 chr7: 2,635,595-2,635,869 , GRCh37.p13 chr7: 2,675,229-2,675,503 TTYH3
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