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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070229inversion1nstd229human GRCh38 chr11: 92,451,554-94,033,544 , GRCh37.p13 chr11: 92,184,720-93,766,710 SNORA32, SNORA18, 30 more genes
    nsv7060154inversion1nstd229human GRCh38 chr11: 89,626,991-96,425,689 , GRCh37.p13 chr11: 89,360,159-96,158,853 LINC02756, OSBPL9P2, 119 more genes
    nsv6914121copy number variation1nstd229human GRCh38 chr11: 89,708,489-94,988,932 , GRCh37.p13 chr11: 89,441,657-94,611,845 SNORA40, PIWIL4-AS1, 89 more genes
    nsv6913192copy number variation1nstd229human GRCh38 chr11: 93,809,001-93,815,600 , GRCh37.p13 chr11: 93,542,167-93,548,766 MED17, VSTM5
    nsv6907347copy number variation1nstd229human GRCh38 chr11: 89,715,432-96,566,090 , GRCh37.p13 chr11: 89,448,600-96,287,584 DISC1FP1, RPL32P25, 120 more genes
    nsv6906069copy number variation1nstd229human GRCh38 chr11: 93,796,866-93,797,406 , GRCh37.p13 chr11: 93,530,032-93,530,572 MED17
    nsv6903423copy number variation1nstd229human GRCh38 chr11: 93,807,257-93,811,615 , GRCh37.p13 chr11: 93,540,423-93,544,781 MED17
    nsv6900323copy number variation1nstd229human GRCh38 chr11: 93,200,748-96,340,159 , GRCh37.p13 chr11: 92,933,914-96,073,323 FGFR3P2, LOC112268080, 67 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
    nsv6474953copy number variation1nstd223human GRCh38 chr11: 93,787,215-93,788,404 , GRCh37.p13 chr11: 93,520,381-93,521,570 MED17
    nsv6462555copy number variation1nstd223human GRCh38 chr11: 93,796,866-93,797,406 , GRCh37.p13 chr11: 93,530,032-93,530,572 MED17
    nsv6459070copy number variation1nstd223human GRCh38 chr11: 92,156,862-95,481,795 , GRCh37.p13 chr11: 91,890,028-95,214,959 FUT4, KDM4D, 66 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6314019copy number variation1nstd102humanUncertain significance GRCh37 chr11: 90,906,452-94,437,087 , GRCh38.p12 chr11: 91,173,284-94,703,921 PGAM1P9, C11orf97, 52 more genes
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6309454copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 93,540,674-93,543,052 , GRCh38.p12 chr11: 93,807,508-93,809,886 MED17
    nsv6309389copy number variation1nstd102humanPathogenic GRCh37 chr11: 93,529,711-93,539,976 , GRCh38.p12 chr11: 93,796,545-93,806,810 MED17
    nsv6309388copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 93,529,566-93,545,240 , GRCh38.p12 chr11: 93,796,400-93,812,074 MED17
    nsv6309240copy number variation1nstd102humanPathogenic GRCh37 chr11: 93,517,670-93,517,939 , GRCh38.p12 chr11: 93,784,504-93,784,773 MED17
    nsv6291431copy number variation1nstd102humanUncertain significance GRCh37 chr11: 93,475,922-93,778,658 , GRCh38.p12 chr11: 93,742,756-94,045,492 LOC101060084, HPRT1P3, 4 more genes
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