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Items: 1 to 20 of 88

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
    nsv5264980copy number variation1nstd204human GRCh38.p13 chr11: 65,876,001-66,092,800 , GRCh37.p13 chr11: 65,643,472-65,860,271 , LOC100420020, 17 more genes
    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
    nsv4576134mobile element insertion1nstd166human GRCh37.p13 chr11: 65,835,956-65,835,956 , GRCh38.p12 chr11: 66,068,485-66,068,485 SF3B2, PACS1
    nsv4453555copy number variation1nstd102humanUncertain significance GRCh38 chr11: 65,866,431-66,347,555 , GRCh37 chr11: 65,633,902-66,115,026 CNIH2, YIF1A, 33 more genes
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 SNORD13F, ZNRD2, 141 more genes
    nsv3956311insertion1nstd168human GRCh38 chr11: 66,059,935-66,093,486 , GRCh37.p13 chr11: 65,827,406-65,860,957 SF3B2, PACS1
    nsv3921639copy number variation1nstd102humanPathogenic NCBI36 chr11: 65,265,478-67,229,716 , GRCh37 chr11: 65,508,902-67,473,140 , GRCh38 chr11: 65,741,431-67,705,669 MIR6860, DOC2GP, 106 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3902272copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 64,501,919-67,129,258 , GRCh38.p12 chr11: 64,734,447-67,361,787 ACTN3, GRK2, 157 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
    nsv3167936inversion1nstd158human GRCh37 chr11: 64,590,560-68,196,411 , GRCh38.p12 chr11: 64,823,088-68,428,943 , ACTN3, 210 more genes
    nsv1592296short tandem repeat2nstd128human GRCh37 chr11: 65,828,266-65,828,284 , GRCh38.p12 chr11: 66,060,795-66,060,813 SF3B2
    nsv1590923short tandem repeat2nstd128human GRCh37 chr11: 65,833,330-65,833,363 , GRCh38.p12 chr11: 66,065,859-66,065,892 SF3B2
    nsv1590922short tandem repeat6nstd128human GRCh37 chr11: 65,821,949-65,821,964 , GRCh38.p12 chr11: 66,054,478-66,054,493 SF3B2
    nsv1590921short tandem repeat4nstd128human GRCh37 chr11: 65,821,651-65,821,664 , GRCh38.p12 chr11: 66,054,180-66,054,193 SF3B2
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