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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5864597copy number variation1nstd209human GRCh38 chr11: 124,015,473-124,025,121 , GRCh37.p13 chr11: 123,886,180-123,895,828 OR10G9, OR10G4
    nsv5857479copy number variation1nstd209human GRCh38 chr11: 124,014,733-124,016,884 , GRCh37.p13 chr11: 123,885,440-123,887,591 OR10G4
    nsv5853910copy number variation2nstd209human GRCh38 chr11: 124,016,585-124,023,077 , GRCh37.p13 chr11: 123,887,292-123,893,784 OR10G4, OR10G9
    nsv5699843mobile element insertion2nstd211human GRCh38 chr11: 124,015,265-124,015,265 , GRCh37.p13 chr11: 123,885,972-123,885,972 OR10G4
    nsv5503511copy number variation1nstd206human GRCh38 chr11: 124,016,182-124,023,364 , GRCh37.p13 chr11: 123,886,889-123,894,071 OR10G9, OR10G4
    nsv5426091mobile element insertion1nstd206human GRCh38 chr11: 124,015,265-124,015,307 , GRCh37.p13 chr11: 123,885,972-123,886,014 OR10G4
    nsv5335363translocation1nstd200human GRCh37 chr11: 123,886,828-123,886,828 , GRCh37 chr11: 123,909,240-123,909,240 , GRCh38.p12 chr11: 124,016,121-124,016,121 , GRCh38.p12 chr11: 124,038,533-124,038,533 OR10G7, OR10G4
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 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
    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
    nsv4499486mobile element insertion1nstd166human GRCh37.p13 chr11: 123,885,954-123,885,954 , GRCh38.p12 chr11: 124,015,247-124,015,247 OR10G4
    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
    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
    nsv4204797copy number variation1nstd166human GRCh37.p13 chr11: 123,886,750-123,894,000 , GRCh38.p12 chr11: 124,016,043-124,023,293 OR10G4, OR10G9
    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
    nsv3923916copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,296,802-124,641,109 , NCBI36 chr11: 119,802,012-124,146,319 , GRCh38 chr11: 120,426,093-124,771,213 OR8B2, OR8G5, 120 more genes
    nsv3923375copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,722,088-134,868,420 , NCBI36 chr11: 116,227,298-134,373,630 , GRCh38 chr11: 116,851,372-134,998,526 VPS26B, LOC105369531, 390 more genes
    nsv3923251copy number variation1nstd102humanPathogenic NCBI36 chr11: 119,891,678-134,450,377 , GRCh38 chr11: 120,515,759-135,075,271 , GRCh37 chr11: 120,386,468-134,945,165 KIRREL3-AS3, OR8B4, 279 more genes
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