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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093915copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,171,709-111,958,707 , GRCh38.p12 chr11: 111,300,984-112,087,983 CRYAB, BTG4, 34 more genes
    nsv7093830copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,171,709-111,959,745 , GRCh38.p12 chr11: 111,300,984-112,089,021 LOC100132078, DLAT, 34 more genes
    nsv7093669copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,171,709-112,104,278 , GRCh38.p12 chr11: 111,300,984-112,233,555 CRYAB, RPS6P16, 43 more genes
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv6917525copy number variation1nstd229human GRCh38 chr11: 111,658,462-111,666,508 , GRCh37.p13 chr11: 111,529,186-111,537,232 SIK2
    nsv6917072copy number variation1nstd229human GRCh38 chr11: 111,624,855-111,630,355 , GRCh37.p13 chr11: 111,495,579-111,501,079 SIK2
    nsv6915620copy number variation1nstd229human GRCh38 chr11: 111,603,861-111,606,033 , GRCh37.p13 chr11: 111,474,585-111,476,757 SIK2
    nsv6912837copy number variation1nstd229human GRCh38 chr11: 111,665,501-111,673,100 , GRCh37.p13 chr11: 111,536,225-111,543,824 SIK2
    nsv6908884copy number variation1nstd229human GRCh38 chr11: 111,594,717-111,615,383 , GRCh37.p13 chr11: 111,465,441-111,486,107 SIK2
    nsv6908820copy number variation1nstd229human GRCh38 chr11: 111,716,883-111,716,928 , GRCh37.p13 chr11: 111,587,607-111,587,652 PPP2R1B, SIK2
    nsv6908645copy number variation1nstd229human GRCh38 chr11: 111,632,734-111,641,772 , GRCh37.p13 chr11: 111,503,458-111,512,496 SIK2
    nsv6908392copy number variation1nstd229human GRCh38 chr11: 111,684,360-111,686,508 , GRCh37.p13 chr11: 111,555,084-111,557,232 SIK2
    nsv6907742copy number variation1nstd229human GRCh38 chr11: 111,697,752-111,712,926 , GRCh37.p13 chr11: 111,568,476-111,583,650 PPP2R1B, SIK2
    nsv6905847copy number variation1nstd229human GRCh38 chr11: 111,609,490-111,613,196 , GRCh37.p13 chr11: 111,480,214-111,483,920 SIK2
    nsv6904419copy number variation1nstd229human GRCh38 chr11: 111,700,343-111,700,445 , GRCh37.p13 chr11: 111,571,067-111,571,169 SIK2, PPP2R1B
    nsv6904030copy number variation1nstd229human GRCh38 chr11: 111,712,101-111,719,400 , GRCh37.p13 chr11: 111,582,825-111,590,124 SIK2, PPP2R1B
    nsv6903209copy number variation1nstd229human GRCh38 chr11: 111,610,113-111,615,065 , GRCh37.p13 chr11: 111,480,837-111,485,789 SIK2
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
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