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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5726112mobile element insertion2nstd211human GRCh38 chr11: 125,262,896-125,262,896 , GRCh37.p13 chr11: 125,132,792-125,132,792 PKNOX2-AS1, PKNOX2
    nsv5555903mobile element insertion1nstd206human GRCh38 chr11: 125,262,896-125,262,947 , GRCh37.p13 chr11: 125,132,792-125,132,843 PKNOX2-AS1, PKNOX2
    nsv5261364copy number variation1nstd204human GRCh38.p13 chr11: 125,265,719-125,266,818 , GRCh37.p13 chr11: 125,135,615-125,136,714 PKNOX2-AS1, PKNOX2
    nsv4981154copy number variation1nstd200human GRCh38 chr11: 125,264,553-125,266,253 , GRCh37.p13 chr11: 125,134,449-125,136,149 PKNOX2-AS1, PKNOX2
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4729382copy number variation1nstd102humanUncertain significance GRCh37 chr11: 124,941,693-125,228,288 , GRCh38.p12 chr11: 125,071,797-125,358,392 SLC37A2, PKNOX2-DT, 5 more genes
    nsv4675832copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576 MIR8052, BLID, 275 more genes
    nsv4675674copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,232,608-134,938,470 , GRCh38.p12 chr11: 124,362,712-135,068,576 FAM118B, PUS3, 184 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4673961copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,226,940-134,944,477 , GRCh38.p12 chr11: 124,357,044-135,074,583 OR8A2P, LOC101929473, 186 more genes
    nsv4606555copy number variation1nstd183human GRCh37 chr11: 124,692,835-125,311,674 , GRCh38.p12 chr11: 124,822,939-125,441,778 HEPN1, TMEM218, 14 more genes
    nsv4599038copy number variation1nstd183human GRCh37 chr11: 124,907,025-125,313,039 , GRCh38.p12 chr11: 125,037,129-125,443,143 FEZ1, PKNOX2, 7 more genes
    nsv4455281copy number variation1nstd102humanPathogenic GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576 NTM-AS1, LOC403312, 369 more genes
    nsv4436748copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169 LINC02098, LOC105369587, 276 more genes
    nsv4371573copy number variation1nstd173human GRCh37 chr11: 124,912,625-125,213,218 , GRCh38.p12 chr11: 125,042,729-125,343,322 PKNOX2, KRT18P59, 5 more genes
    nsv4367632copy number variation1nstd173human GRCh37 chr11: 124,912,625-125,222,213 , GRCh38.p12 chr11: 125,042,729-125,352,317 PKNOX2-AS1, SLC37A2, 5 more genes
    nsv4349506copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591 LOC107984407, DCPS, 394 more genes
    nsv4349045copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169 MPZL3, ADAMTS8, 393 more genes
    nsv4206975copy number variation1nstd166human GRCh37.p13 chr11: 125,134,449-125,136,149 , GRCh38.p12 chr11: 125,264,553-125,266,253 PKNOX2-AS1, PKNOX2
    nsv3924566copy number variation1nstd102humanPathogenic GRCh38 chr11: 120,507,265-134,576,266 , NCBI36 chr11: 119,883,184-133,951,370 , GRCh37 chr11: 120,377,974-134,446,160 CCDC15-DT, LOC105369544, 271 more genes
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