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Items: 1 to 20 of 327

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094019copy number variation1nstd102humanUncertain significance GRCh37 chr11: 88,027,174-89,018,142 , GRCh38.p12 chr11: 88,294,006-89,284,974 GRM5, RNU6-16P, 5 more genes
    nsv7069436inversion1nstd229human GRCh38 chr11: 85,936,971-89,461,473 , GRCh37.p13 chr11: 85,648,014-89,194,641 , RNU6-1135P, 45 more genes
    nsv6917567copy number variation1nstd229human GRCh38 chr11: 88,411,182-88,421,471 , GRCh37.p13 chr11: 88,144,350-88,154,639 LOC101929174
    nsv6917057copy number variation1nstd229human GRCh38 chr11: 88,334,501-88,366,800 , GRCh37.p13 chr11: 88,067,669-88,099,968 CTSC, LOC101929174
    nsv6916671copy number variation1nstd229human GRCh38 chr11: 88,370,270-88,376,572 , GRCh37.p13 chr11: 88,103,438-88,109,740 LOC101929174
    nsv6914401copy number variation1nstd229human GRCh38 chr11: 88,408,094-88,414,830 , GRCh37.p13 chr11: 88,141,262-88,147,998 GAPDHP70, LOC101929174
    nsv6913748copy number variation1nstd229human GRCh38 chr11: 88,182,152-88,370,144 , GRCh37.p13 chr11: 87,915,320-88,103,312 CTSC, LOC101929174
    nsv6912967copy number variation1nstd229human GRCh38 chr11: 88,353,010-88,424,337 , GRCh37.p13 chr11: 88,086,178-88,157,505 LOC101929174, GAPDHP70
    nsv6909113copy number variation1nstd229human GRCh38 chr11: 88,411,201-88,422,900 , GRCh37.p13 chr11: 88,144,369-88,156,068 LOC101929174
    nsv6908694copy number variation1nstd229human GRCh38 chr11: 88,348,133-88,353,800 , GRCh37.p13 chr11: 88,081,301-88,086,968 LOC101929174
    nsv6907681copy number variation1nstd229human GRCh38 chr11: 88,223,355-88,425,298 , GRCh37.p13 chr11: 87,956,523-88,158,466 CTSC, GAPDHP70, 1 more genes
    nsv6903752copy number variation1nstd229human GRCh38 chr11: 88,403,726-88,414,637 , GRCh37.p13 chr11: 88,136,894-88,147,805 LOC101929174, GAPDHP70
    nsv6901172copy number variation1nstd229human GRCh38 chr11: 88,365,184-88,371,771 , GRCh37.p13 chr11: 88,098,352-88,104,939 LOC101929174
    nsv6899916copy number variation1nstd229human GRCh38 chr11: 88,343,943-88,347,455 , GRCh37.p13 chr11: 88,077,111-88,080,623 LOC101929174
    nsv6899156copy number variation1nstd229human GRCh38 chr11: 88,323,101-88,376,300 , GRCh37.p13 chr11: 88,056,269-88,109,468 CTSC, LOC101929174
    nsv6898119copy number variation1nstd229human GRCh38 chr11: 88,412,981-88,420,173 , GRCh37.p13 chr11: 88,146,149-88,153,341 LOC101929174
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6592929inversion1nstd223human GRCh38 chr11: 88,385,288-88,386,792 , GRCh37.p13 chr11: 88,118,456-88,119,960 LOC101929174
    nsv6474217copy number variation1nstd223human GRCh38 chr11: 88,365,184-88,371,766 , GRCh37.p13 chr11: 88,098,352-88,104,934 LOC101929174
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