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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5882919copy number variation1nstd209human GRCh38 chr1: 156,556,912-156,559,142 , GRCh37.p13 chr1: 156,526,704-156,528,934 IQGAP3
    nsv5617320insertion1nstd207human GRCh38 chr1: 156,557,722-156,557,722 , GRCh37.p13 chr1: 156,527,514-156,527,514 IQGAP3
    nsv5606019insertion1nstd207human GRCh38 chr1: 156,558,077-156,558,077 , GRCh37.p13 chr1: 156,527,869-156,527,869 IQGAP3
    nsv5604709insertion1nstd207human GRCh38 chr1: 156,557,654-156,557,654 , GRCh37.p13 chr1: 156,527,446-156,527,446 IQGAP3
    nsv5580219copy number variation1nstd207human GRCh38 chr1: 156,556,912-156,559,142 , GRCh37.p13 chr1: 156,526,704-156,528,934 IQGAP3
    nsv5428039copy number variation1nstd206human GRCh38 chr1: 156,522,124-156,525,938 , GRCh37.p13 chr1: 156,491,916-156,495,730 IQGAP3
    nsv5420760copy number variation1nstd206human GRCh38 chr1: 156,556,911-156,559,163 , GRCh37.p13 chr1: 156,526,703-156,528,955 IQGAP3
    nsv5383000copy number variation2nstd186human GRCh37 chr1: 156,526,723-156,528,935 , GRCh38.p12 chr1: 156,556,931-156,559,143 IQGAP3
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5344754translocation1nstd200human GRCh37 chr1: 156,491,916-156,491,916 , GRCh37 chr1: 156,495,730-156,495,730 , GRCh38.p12 chr1: 156,525,938-156,525,938 , GRCh38.p12 chr1: 156,522,124-156,522,124 IQGAP3
    nsv5329257translocation1nstd204human GRCh38.p13 chr1: 156,559,143-156,559,143 , GRCh38.p13 chr1: 156,556,931-156,556,931 , GRCh37.p13 chr1: 156,526,723-156,526,723 , GRCh37.p13 chr1: 156,528,935-156,528,935 IQGAP3
    nsv5299319copy number variation1nstd204human GRCh38.p13 chr1: 156,522,122-156,525,939 , GRCh37.p13 chr1: 156,491,914-156,495,731 IQGAP3
    nsv5296423copy number variation1nstd204human GRCh38.p13 chr1: 156,521,510-156,523,578 , GRCh37.p13 chr1: 156,491,302-156,493,370 IQGAP3
    nsv5295917copy number variation1nstd204human GRCh37.p13 chr1: 156,469,049-156,626,622 , GRCh38.p13 chr1: 156,499,257-156,656,830 MEF2D, GPATCH4, 7 more genes
    nsv5285848copy number variation1nstd204human GRCh38.p13 chr1: 156,544,017-156,575,007 , GRCh37.p13 chr1: 156,513,809-156,544,799 IQGAP3
    nsv5219788copy number variation1nstd204human GRCh38.p13 chr1: 156,566,421-156,570,650 , GRCh37.p13 chr1: 156,536,213-156,540,442 IQGAP3
    nsv5219329copy number variation1nstd204human GRCh37.p13 chr1: 156,529,193-156,625,692 , GRCh38.p13 chr1: 156,559,401-156,655,900 GPATCH4, HAPLN2, 6 more genes
    nsv5216438copy number variation1nstd204human GRCh38.p13 chr1: 156,544,701-156,556,900 , GRCh37.p13 chr1: 156,514,493-156,526,692 IQGAP3
    nsv5215079copy number variation1nstd204human GRCh38.p13 chr1: 156,545,564-156,547,892 , GRCh37.p13 chr1: 156,515,356-156,517,684 IQGAP3
    nsv5213440copy number variation1nstd204human GRCh38.p13 chr1: 156,556,901-156,557,300 , GRCh37.p13 chr1: 156,526,693-156,527,092 IQGAP3
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