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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5494028copy number variation1nstd206human GRCh38 chr11: 74,225,600-74,828,943 , GRCh37.p13 chr11: 73,936,645-74,539,988 RNF169, MIR4696, 19 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
    nsv5308371copy number variation1nstd204human GRCh37.p13 chr11: 74,108,683-74,180,713 , GRCh38.p13 chr11: 74,397,638-74,469,668 KCNE3, PGM2L1, 1 more genes
    nsv4987306copy number variation1nstd200human GRCh38 chr11: 74,397,640-74,469,668 , GRCh37.p13 chr11: 74,108,685-74,180,713 MIR548AL, PGM2L1, 1 more genes
    nsv4836189copy number variation1nstd200human GRCh37 chr11: 74,108,685-74,180,713 , GRCh38.p12 chr11: 74,397,640-74,469,668 KCNE3, PGM2L1, 1 more genes
    nsv4605206copy number variation1nstd183human GRCh37 chr11: 74,114,801-74,177,921 , GRCh38.p12 chr11: 74,403,756-74,466,876 KCNE3
    nsv4574169mobile element insertion1nstd166human GRCh37.p13 chr11: 74,176,779-74,176,779 , GRCh38.p12 chr11: 74,465,734-74,465,734 KCNE3
    nsv4418797copy number variation1nstd174human GRCh37 chr11: 73,936,645-74,539,988 , GRCh38.p12 chr11: 74,225,600-74,828,943 POLD3, CHRDL2, 19 more genes
    nsv4337133sequence alteration1nstd166human GRCh37.p13 chr11: 74,175,761-74,176,631 , GRCh38.p12 chr11: 74,464,716-74,465,586 KCNE3
    nsv3916301copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216 RN7SL786P, LIPT2-AS1, 146 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 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
    nsv3908488copy number variation1nstd102humanBenign GRCh37 chr11: 74,109,166-74,180,489 , GRCh38.p12 chr11: 74,398,121-74,469,444 PGM2L1, KCNE3, 1 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
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 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
    nsv3143353copy number variation1nstd151human GRCh37 chr11: 74,109,093-74,168,613 , GRCh38.p12 chr11: 74,398,048-74,457,568 PGM2L1, KCNE3, 1 more genes
    nsv3142081copy number variation1nstd151human GRCh37 chr11: 71,668,270-74,638,536 , GRCh38.p12 chr11: 71,957,224-74,927,491 , RPL36AP38, 92 more genes
    nsv2787673copy number variation1nstd132human NCBI36 chr11: 73,786,814-73,858,137 , GRCh37.p13 chr11: 74,109,166-74,180,489 , GRCh38.p12 chr11: 74,398,121-74,469,444 KCNE3, PGM2L1, 1 more genes
    nsv2786158copy number variation1nstd132human NCBI36 chr11: 73,782,753-73,861,481 , GRCh37.p13 chr11: 74,105,105-74,183,833 , GRCh38.p12 chr11: 74,394,060-74,472,788 PGM2L1, KCNE3, 1 more genes
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