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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 PHF7, SEMA3G, 47 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv6718083copy number variation1nstd229human GRCh38 chr3: 52,315,001-52,487,400 , GRCh37.p13 chr3: 52,349,017-52,521,416 BAP1, NISCH, 5 more genes
    nsv6712251copy number variation1nstd229human GRCh38 chr3: 52,386,019-52,420,329 , GRCh37.p13 chr3: 52,420,035-52,454,345 PHF7, DNAH1, 1 more genes
    nsv6711686copy number variation1nstd229human GRCh38 chr3: 51,850,901-52,533,900 , GRCh37.p13 chr3: 51,884,917-52,567,916 LOC105377088, GLYCTK-AS1, 37 more genes
    nsv6700890copy number variation1nstd229human GRCh38 chr3: 52,237,701-52,533,900 , GRCh37.p13 chr3: 52,271,717-52,567,916 STAB1, TWF2, 16 more genes
    nsv6369827copy number variation1nstd223human GRCh38 chr3: 52,164,358-54,467,618 , GRCh37.p13 chr3: 52,198,374-54,501,645 SEMA3G, STAB1, 61 more genes
    nsv6358449copy number variation1nstd223human GRCh38 chr3: 52,412,957-52,447,789 , GRCh37.p13 chr3: 52,446,973-52,481,805 SEMA3G, PHF7
    nsv6311694copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,441,964-52,443,894 , GRCh38.p12 chr3: 52,407,948-52,409,878 BAP1, PHF7
    nsv6156092copy number variation1nstd214human GRCh38 chr3: 52,410,462-52,410,526 , GRCh37.p13 chr3: 52,444,478-52,444,542 BAP1, PHF7
    nsv6151642copy number variation1nstd214human GRCh38 chr3: 52,413,113-52,413,167 , GRCh37.p13 chr3: 52,447,129-52,447,183 PHF7
    nsv6134815copy number variation1nstd213human GRCh37 chr3: 52,350,000-53,060,001 , GRCh38.p12 chr3: 52,315,984-53,025,985 ITIH1, ITIH3, 32 more genes
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5315916copy number variation1nstd204human GRCh38.p13 chr3: 52,412,020-52,414,756 , GRCh37.p13 chr3: 52,446,036-52,448,772 PHF7
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4914344copy number variation1nstd200human GRCh38 chr3: 52,386,019-52,420,329 , GRCh37.p13 chr3: 52,420,035-52,454,345 BAP1, DNAH1, 1 more genes
    nsv4911374copy number variation1nstd200human GRCh38 chr3: 52,416,480-52,419,060 , GRCh37.p13 chr3: 52,450,496-52,453,076 PHF7
    nsv4911373copy number variation1nstd200human GRCh38 chr3: 52,412,029-52,414,749 , GRCh37.p13 chr3: 52,446,045-52,448,765 PHF7
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