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Items: 1 to 20 of 1479

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137937insertion1nstd232human GRCh37.p13 chr2: 40,424,955-40,424,955 , GRCh38.p12 chr2: 40,197,815-40,197,815 SLC8A1, SLC8A1-AS1
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7055881inversion1nstd229human GRCh38 chr2: 40,471,307-40,471,380 , GRCh37.p13 chr2: 40,698,447-40,698,520 SLC8A1
    nsv7043959inversion1nstd229human GRCh38 chr2: 40,347,287-40,472,870 , GRCh37.p13 chr2: 40,574,427-40,700,010 SLC8A1
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv7039581inversion1nstd229human GRCh38 chr2: 40,471,473-40,566,307 , GRCh37.p13 chr2: 40,698,613-40,793,447 LOC101929667, SLC8A1
    nsv6677225copy number variation1nstd229human GRCh38 chr2: 40,296,703-40,417,353 , GRCh37.p13 chr2: 40,523,843-40,644,493 SLC8A1
    nsv6677156copy number variation1nstd229human GRCh38 chr2: 40,493,601-40,497,000 , GRCh37.p13 chr2: 40,720,741-40,724,140 SLC8A1
    nsv6677152copy number variation1nstd229human GRCh38 chr2: 40,164,263-40,167,869 , GRCh37.p13 chr2: 40,391,403-40,395,009 SLC8A1-AS1, SLC8A1
    nsv6677007copy number variation1nstd229human GRCh38 chr2: 40,359,501-40,385,100 , GRCh37.p13 chr2: 40,586,641-40,612,240 SLC8A1
    nsv6676907copy number variation1nstd229human GRCh38 chr2: 40,216,201-40,217,500 , GRCh37.p13 chr2: 40,443,341-40,444,640 SLC8A1-AS1, SLC8A1
    nsv6676607copy number variation1nstd229human GRCh38 chr2: 40,212,848-40,219,316 , GRCh37.p13 chr2: 40,439,988-40,446,456 SLC8A1, SLC8A1-AS1
    nsv6676480copy number variation1nstd229human GRCh38 chr2: 40,334,301-40,386,200 , GRCh37.p13 chr2: 40,561,441-40,613,340 SLC8A1
    nsv6676396copy number variation1nstd229human GRCh38 chr2: 40,403,901-40,421,461 , GRCh37.p13 chr2: 40,631,041-40,648,601 SLC8A1
    nsv6676116copy number variation1nstd229human GRCh38 chr2: 40,341,194-40,382,531 , GRCh37.p13 chr2: 40,568,334-40,609,671 SLC8A1
    nsv6675969copy number variation1nstd229human GRCh38 chr2: 40,106,601-40,108,800 , GRCh37.p13 chr2: 40,333,741-40,335,940 SLC8A1-AS1, SLC8A1
    nsv6675740copy number variation1nstd229human GRCh38 chr2: 40,375,031-40,377,159 , GRCh37.p13 chr2: 40,602,171-40,604,299 SLC8A1
    nsv6675473copy number variation1nstd229human GRCh38 chr2: 40,494,101-40,497,000 , GRCh37.p13 chr2: 40,721,241-40,724,140 SLC8A1
    nsv6674264copy number variation1nstd229human GRCh38 chr2: 40,196,059-40,206,029 , GRCh37.p13 chr2: 40,423,199-40,433,169 SLC8A1, SLC8A1-AS1
    nsv6674188copy number variation1nstd229human GRCh38 chr2: 40,457,131-40,459,378 , GRCh37.p13 chr2: 40,684,271-40,686,518 SLC8A1
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