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Items: 1 to 20 of 413

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142374copy number variation1nstd232human GRCh37.p13 chr16: 23,328,026-23,328,112 , GRCh38.p12 chr16: 23,316,705-23,316,791 SCNN1B
    nsv7141440copy number variation1nstd232human GRCh37.p13 chr16: 23,344,418-23,344,469 , GRCh38.p12 chr16: 23,333,097-23,333,148 SCNN1B
    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
    nsv7094827copy number variation1nstd102humanUncertain significance GRCh37 chr16: 23,193,865-23,652,612 , GRCh38.p12 chr16: 23,182,544-23,641,291 PALB2, SCNN1G, 10 more genes
    nsv7069500inversion1nstd229human GRCh38 chr16: 23,351,920-23,355,885 , GRCh37.p13 chr16: 23,363,241-23,367,206 SCNN1B
    nsv7066287inversion1nstd229human GRCh38 chr16: 23,092,980-23,338,256 , GRCh37.p13 chr16: 23,104,301-23,349,577 SCNN1B, USP31, 1 more genes
    nsv7065139inversion1nstd229human GRCh38 chr16: 23,334,897-23,341,655 , GRCh37.p13 chr16: 23,346,218-23,352,976 SCNN1B
    nsv7062391inversion1nstd229human GRCh38 chr16: 23,338,135-23,338,330 , GRCh37.p13 chr16: 23,349,456-23,349,651 SCNN1B
    nsv7060882inversion1nstd229human GRCh38 chr16: 23,327,885-23,341,382 , GRCh37.p13 chr16: 23,339,206-23,352,703 SCNN1B
    nsv7060602inversion1nstd229human GRCh38 chr16: 22,087,809-24,116,610 , GRCh37.p13 chr16: 22,099,130-24,127,931 RRN3P3, MFSD13B, 34 more genes
    nsv7058979inversion1nstd229human GRCh38 chr16: 23,348,132-23,352,115 , GRCh37.p13 chr16: 23,359,453-23,363,436 SCNN1B
    nsv7058720inversion1nstd229human GRCh38 chr16: 21,529,628-23,453,946 , GRCh37.p13 chr16: 21,540,949-23,465,267 CDR2-DT, LOC105371131, 40 more genes
    nsv6997155copy number variation1nstd229human GRCh38 chr16: 23,343,501-23,348,700 , GRCh37.p13 chr16: 23,354,822-23,360,021 SCNN1B
    nsv6995391copy number variation1nstd229human GRCh38 chr16: 23,334,773-23,534,768 , GRCh37.p13 chr16: 23,346,094-23,546,089 COG7, RN7SKP23, 4 more genes
    nsv6994659copy number variation1nstd229human GRCh38 chr16: 23,321,184-23,326,314 , GRCh37.p13 chr16: 23,332,505-23,337,635 SCNN1B
    nsv6994228copy number variation1nstd229human GRCh38 chr16: 23,333,097-23,333,149 , GRCh37.p13 chr16: 23,344,418-23,344,470 SCNN1B
    nsv6994064copy number variation1nstd229human GRCh38 chr16: 23,366,735-23,367,306 , GRCh37.p13 chr16: 23,378,056-23,378,627 SCNN1B
    nsv6992492copy number variation1nstd229human GRCh38 chr16: 23,206,524-23,287,486 , GRCh37.p13 chr16: 23,217,845-23,298,807 SCNN1G, SCNN1B
    nsv6989656copy number variation1nstd229human GRCh38 chr16: 23,325,535-23,325,576 , GRCh37.p13 chr16: 23,336,856-23,336,897 SCNN1B
    nsv6989306copy number variation1nstd229human GRCh38 chr16: 23,260,001-23,277,900 , GRCh37.p13 chr16: 23,271,322-23,289,221 SCNN1B
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