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Items: 1 to 20 of 947

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143387copy number variation1nstd232human GRCh37.p13 chr16: 24,126,593-24,126,651 , GRCh38.p12 chr16: 24,115,272-24,115,330 PRKCB
    nsv7139248copy number variation1nstd232human GRCh37.p13 chr16: 24,126,508-24,126,579 , GRCh38.p12 chr16: 24,115,187-24,115,258 PRKCB
    nsv7138728copy number variation1nstd232human GRCh37.p13 chr16: 23,993,112-23,993,211 , GRCh38.p12 chr16: 23,981,791-23,981,890 PRKCB
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7072745inversion1nstd229human GRCh38 chr16: 24,126,533-24,127,580 , GRCh37.p13 chr16: 24,137,854-24,138,901 PRKCB
    nsv7069743inversion1nstd229human GRCh38 chr16: 24,051,079-24,064,786 , GRCh37.p13 chr16: 24,062,400-24,076,107 PRKCB
    nsv7069063inversion1nstd229human GRCh38 chr16: 23,921,573-23,929,418 , GRCh37.p13 chr16: 23,932,894-23,940,739 PRKCB
    nsv7061607inversion1nstd229human GRCh38 chr16: 23,922,051-23,925,605 , GRCh37.p13 chr16: 23,933,372-23,936,926 PRKCB
    nsv7061059inversion1nstd229human GRCh38 chr16: 23,459,969-24,877,943 , GRCh37.p13 chr16: 23,471,290-24,889,264 LOC105371143, CHP2, 20 more genes
    nsv7060602inversion1nstd229human GRCh38 chr16: 22,087,809-24,116,610 , GRCh37.p13 chr16: 22,099,130-24,127,931 RRN3P3, MFSD13B, 34 more genes
    nsv6997130copy number variation1nstd229human GRCh38 chr16: 23,977,755-23,984,719 , GRCh37.p13 chr16: 23,989,076-23,996,040 PRKCB
    nsv6997037copy number variation1nstd229human GRCh38 chr16: 23,981,704-23,985,426 , GRCh37.p13 chr16: 23,993,025-23,996,747 PRKCB
    nsv6996503copy number variation1nstd229human GRCh38 chr16: 24,075,295-24,076,167 , GRCh37.p13 chr16: 24,086,616-24,087,488 PRKCB
    nsv6995680copy number variation1nstd229human GRCh38 chr16: 24,011,064-24,013,735 , GRCh37.p13 chr16: 24,022,385-24,025,056 PRKCB
    nsv6995160copy number variation1nstd229human GRCh38 chr16: 23,899,566-23,899,873 , GRCh37.p13 chr16: 23,910,887-23,911,194 PRKCB
    nsv6994918copy number variation1nstd229human GRCh38 chr16: 24,115,187-24,115,396 , GRCh37.p13 chr16: 24,126,508-24,126,717 PRKCB
    nsv6994812copy number variation1nstd229human GRCh38 chr16: 23,946,606-23,946,624 , GRCh37.p13 chr16: 23,957,927-23,957,945 PRKCB
    nsv6993297copy number variation1nstd229human GRCh38 chr16: 23,892,760-23,899,184 , GRCh37.p13 chr16: 23,904,081-23,910,505 PRKCB
    nsv6992933copy number variation1nstd229human GRCh38 chr16: 23,856,273-23,883,574 , GRCh37.p13 chr16: 23,867,594-23,894,895 PRKCB
    nsv6992438copy number variation1nstd229human GRCh38 chr16: 23,922,001-23,930,900 , GRCh37.p13 chr16: 23,933,322-23,942,221 PRKCB
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