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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7059023inversion1nstd229human GRCh38 chr11: 121,250,599-123,864,348 , GRCh37.p13 chr11: 121,121,308-123,735,056 MIR4493, SF3A3P2, 49 more genes
    nsv6906904copy number variation1nstd229human GRCh38 chr11: 122,109,467-122,113,664 , GRCh37.p13 chr11: 121,980,175-121,984,372 MIR100HG, BLID
    nsv6591553inversion1nstd223human GRCh38 chr11: 119,568,183-123,189,997 , GRCh37.p13 chr11: 119,438,894-123,060,705 UBASH3B, LOC105369529, 66 more genes
    nsv6584901inversion1nstd223human GRCh38 chr11: 120,551,312-124,267,280 , GRCh37.p13 chr11: 120,422,021-124,137,176 RNU6-256P, CLMP, 85 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv5704317mobile element insertion1nstd211human GRCh38 chr11: 122,115,503-122,115,503 , GRCh37.p13 chr11: 121,986,211-121,986,211 BLID, MIR100HG
    nsv5417182mobile element insertion1nstd206human GRCh38 chr11: 122,115,503-122,115,554 , GRCh37.p13 chr11: 121,986,211-121,986,262 MIR100HG, BLID
    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
    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
    nsv3956358copy number variation1nstd168human GRCh38 chr11: 122,101,992-122,128,653 , GRCh37.p13 chr11: 121,972,700-121,999,361 BLID, MIR100HG
    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
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