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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5510703copy number variation1nstd206human GRCh38 chr11: 133,780,000-133,880,364 , GRCh37.p13 chr11: 133,649,895-133,750,259 LOC283172, LINC02743, 1 more genes
    nsv4974158copy number variation1nstd200human GRCh38 chr11: 133,741,120-133,866,238 , GRCh37.p13 chr11: 133,611,015-133,736,133 LINC02743, SPATA19, 1 more genes
    nsv4835755copy number variation1nstd200human GRCh37 chr11: 133,667,874-133,668,149 , GRCh38.p12 chr11: 133,797,979-133,798,254 LINC02743
    nsv4729098copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 130,128,323-134,938,470 , GRCh38.p12 chr11: 130,258,428-135,068,576 BAK1P2, OPCML, 56 more genes
    nsv4729012copy number variation1nstd102humanPathogenic GRCh37 chr11: 127,602,115-134,938,470 , GRCh38.p12 chr11: 127,732,220-135,068,576 LINC02706, APLP2, 92 more genes
    nsv4728891copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,785,487-134,938,470 , GRCh38.p12 chr11: 125,915,592-135,068,576 ARHGAP32, NAP1L1P1, 125 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
    nsv4675571copy number variation1nstd102humanUncertain significance GRCh37 chr11: 131,327,161-134,938,470 , GRCh38.p12 chr11: 131,457,267-135,068,576 SNORD153, LOC105369587, 33 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
    nsv4455332copy number variation1nstd102humanPathogenic GRCh37 chr11: 130,969,272-134,938,470 , GRCh38.p12 chr11: 131,099,377-135,068,576 LOC107984412, LINC02743, 36 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
    nsv4417747copy number variation1nstd174human GRCh37 chr11: 133,607,239-133,740,141 , GRCh38.p12 chr11: 133,737,344-133,870,246 LINC02743, SPATA19, 1 more genes
    nsv4350042copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,446,101-134,904,063 , GRCh38.p12 chr11: 125,576,205-135,034,169 SNX19, TP53AIP1, 138 more genes
    nsv4349788copy number variation1nstd102humanPathogenic GRCh37 chr11: 133,325,079-134,157,243 , GRCh38.p12 chr11: 133,455,184-134,287,349 LINC02743, IGSF9B, 15 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
    nsv4203612copy number variation1nstd166human GRCh37.p13 chr11: 133,667,874-133,668,149 , GRCh38.p12 chr11: 133,797,979-133,798,254 LINC02743
    nsv3924653copy number variation1nstd102humanPathogenic NCBI36 chr11: 126,979,765-134,373,558 , GRCh38 chr11: 127,604,660-134,998,454 , GRCh37 chr11: 127,474,555-134,868,348 ZNF123P, ST14, 91 more genes
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