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Items: 1 to 20 of 544

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056909inversion1nstd229human GRCh38 chr5: 26,896,759-26,900,553 , GRCh37.p13 chr5: 26,896,868-26,900,662 CDH9
    nsv7047140inversion1nstd229human GRCh38 chr5: 21,512,061-29,406,624 , GRCh37.p13 chr5: 21,512,170-29,406,731 AKTIPP2, RNU4-43P, 48 more genes
    nsv7041482inversion1nstd229human GRCh38 chr5: 26,894,223-26,896,925 , GRCh37.p13 chr5: 26,894,332-26,897,034 CDH9
    nsv7040926inversion1nstd229human GRCh38 chr5: 25,459,082-30,588,429 , GRCh37.p13 chr5: 25,459,191-30,588,536 LOC105374703, CCNB3P1, 32 more genes
    nsv6777151copy number variation1nstd229human GRCh38 chr5: 26,920,037-26,932,213 , GRCh37.p13 chr5: 26,920,145-26,932,321 CDH9
    nsv6776971copy number variation1nstd229human GRCh38 chr5: 26,938,765-26,944,075 , GRCh37.p13 chr5: 26,938,873-26,944,182 CDH9
    nsv6775856copy number variation1nstd229human GRCh38 chr5: 26,915,949-26,916,116 , GRCh37.p13 chr5: 26,916,057-26,916,224 CDH9
    nsv6775400copy number variation1nstd229human GRCh38 chr5: 26,760,757-27,463,793 , GRCh37.p13 chr5: 26,760,866-27,463,900 LOC105374695, RNU6-738P, 1 more genes
    nsv6773225copy number variation1nstd229human GRCh38 chr5: 26,880,112-26,893,209 , GRCh37.p13 chr5: 26,880,221-26,893,318 CDH9
    nsv6772821copy number variation1nstd229human GRCh38 chr5: 26,952,082-26,955,960 , GRCh37.p13 chr5: 26,952,189-26,956,067 CDH9
    nsv6771985copy number variation1nstd229human GRCh38 chr5: 27,018,219-27,018,389 , GRCh37.p13 chr5: 27,018,326-27,018,496 CDH9
    nsv6771783copy number variation1nstd229human GRCh38 chr5: 27,027,623-27,033,844 , GRCh37.p13 chr5: 27,027,730-27,033,951 CDH9
    nsv6769917copy number variation1nstd229human GRCh38 chr5: 27,016,355-27,018,018 , GRCh37.p13 chr5: 27,016,462-27,018,125 CDH9
    nsv6767756copy number variation1nstd229human GRCh38 chr5: 27,003,373-27,006,549 , GRCh37.p13 chr5: 27,003,480-27,006,656 CDH9
    nsv6767010copy number variation1nstd229human GRCh38 chr5: 26,970,631-26,970,821 , GRCh37.p13 chr5: 26,970,738-26,970,928 CDH9
    nsv6766732copy number variation1nstd229human GRCh38 chr5: 26,946,954-26,948,820 , GRCh37.p13 chr5: 26,947,061-26,948,927 CDH9
    nsv6766363copy number variation1nstd229human GRCh38 chr5: 27,018,604-27,020,454 , GRCh37.p13 chr5: 27,018,711-27,020,561 CDH9
    nsv6766076copy number variation1nstd229human GRCh38 chr5: 26,908,301-26,909,900 , GRCh37.p13 chr5: 26,908,409-26,910,008 CDH9
    nsv6765052copy number variation1nstd229human GRCh38 chr5: 26,959,373-26,967,032 , GRCh37.p13 chr5: 26,959,480-26,967,139 CDH9
    nsv6764765copy number variation1nstd229human GRCh38 chr5: 26,888,973-26,909,010 , GRCh37.p13 chr5: 26,889,082-26,909,118 CDH9
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