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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093682copy number variation1nstd102humanUncertain significance GRCh37 chr11: 30,253,450-32,460,464 , GRCh38.p12 chr11: 30,231,903-32,438,918 ARL14EP, PAX6, 28 more genes
    nsv7070141inversion1nstd229human GRCh38 chr11: 29,327,534-32,366,322 , GRCh37.p13 chr11: 29,349,081-32,387,868 PAX6, PAUPAR, 35 more genes
    nsv7059455inversion1nstd229human GRCh38 chr11: 31,983,152-32,043,452 , GRCh37.p13 chr11: 32,004,698-32,064,998 LOC105376613, LINC03031, 1 more genes
    nsv6912743copy number variation1nstd229human GRCh38 chr11: 32,038,136-32,041,918 , GRCh37.p13 chr11: 32,059,682-32,063,464 LOC105376613, LINC03031
    nsv6905588copy number variation1nstd229human GRCh38 chr11: 32,033,126-32,293,899 , GRCh37.p13 chr11: 32,054,672-32,315,445 LINC03031, LOC107984322, 6 more genes
    nsv6902589copy number variation1nstd229human GRCh38 chr11: 32,039,690-32,039,878 , GRCh37.p13 chr11: 32,061,236-32,061,424 LINC03031
    nsv6638023copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766 THEM7P, LOC105376624, 92 more genes
    nsv6637271copy number variation1nstd102humanUncertain significance GRCh37 chr11: 31,736,984-32,119,792 , GRCh38.p12 chr11: 31,715,436-32,098,246 LOC101928385, RCN1, 8 more genes
    nsv6637169copy number variation1nstd102humanUncertain significance GRCh37 chr11: 32,044,970-32,153,712 , GRCh38.p12 chr11: 32,023,424-32,132,166 EIF4A2P5, LOC101928385, 4 more genes
    nsv6443576copy number variation1nstd223human GRCh38 chr11: 32,039,755-32,048,560 , GRCh37.p13 chr11: 32,061,301-32,070,106 LINC03031, LOC105376613
    nsv6309193copy number variation1nstd102humanUncertain significance GRCh37 chr11: 31,669,269-32,460,464 , GRCh38.p12 chr11: 31,647,721-32,438,918 LOC107984322, PAX6-AS1, 13 more genes
    nsv6088777insertion1nstd212human GRCh38 chr11: 32,037,252-32,037,252 , GRCh37.p13 chr11: 32,058,798-32,058,798 LINC03031
    nsv5541785insertion1nstd206human GRCh38 chr11: 32,037,298-32,037,324 , GRCh37.p13 chr11: 32,058,844-32,058,870 LINC03031
    nsv5499833copy number variation1nstd206human GRCh38 chr11: 31,402,762-32,071,010 , GRCh37.p13 chr11: 31,424,309-32,092,556 LOC107984420, DNAJC24, 8 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4986939copy number variation1nstd200human GRCh38 chr11: 32,038,134-32,041,914 , GRCh37.p13 chr11: 32,059,680-32,063,460 LOC105376613, LINC03031
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
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