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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049500inversion1nstd229human GRCh38 chr2: 3,572,568-6,665,412 , GRCh37.p13 chr2: 3,620,158-6,805,544 LOC105373393, LOC112268411, 33 more genes
    nsv7046036inversion1nstd229human GRCh38 chr2: 3,570,134-6,661,034 , GRCh37.p13 chr2: 3,617,724-6,801,166 MIR7515, LOC112268411, 33 more genes
    nsv7044096inversion1nstd229human GRCh38 chr2: 5,896,641-9,131,731 , GRCh37.p13 chr2: 6,036,773-9,271,860 LOC105373407, LOC107985847, 48 more genes
    nsv6677695copy number variation1nstd229human GRCh38 chr2: 6,154,901-7,419,900 , GRCh37.p13 chr2: 6,295,033-7,560,031 NRIR, LINC00487, 20 more genes
    nsv6676653copy number variation1nstd229human GRCh38 chr2: 6,629,929-6,641,101 , GRCh37.p13 chr2: 6,770,061-6,781,233 LINC01246
    nsv6672458copy number variation1nstd229human GRCh38 chr2: 6,098,503-6,806,437 , GRCh37.p13 chr2: 6,238,635-6,946,568 LOC105373401, PIK3CDP1, 9 more genes
    nsv6668408copy number variation1nstd229human GRCh38 chr2: 6,632,294-6,961,758 , GRCh37.p13 chr2: 6,772,426-7,101,889 MIR7515, CMPK2, 8 more genes
    nsv6667095copy number variation1nstd229human GRCh38 chr2: 6,630,219-6,631,747 , GRCh37.p13 chr2: 6,770,351-6,771,879 LINC01246
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6661381copy number variation1nstd229human GRCh38 chr2: 6,459,726-6,974,378 , GRCh37.p13 chr2: 6,599,858-7,114,509 LOC107985845, LINC01246, 11 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6636502copy number variation1nstd102humanUncertain significance GRCh37 chr2: 6,765,428-7,101,997 , GRCh38.p12 chr2: 6,625,296-6,961,866 LOC105373404, MIR7515HG, 8 more genes
    nsv6350552copy number variation1nstd223human GRCh38 chr2: 6,098,503-6,806,437 , GRCh37.p13 chr2: 6,238,635-6,946,568 LINC00487, LOC105373401, 9 more genes
    nsv6340020copy number variation1nstd223human GRCh38 chr2: 6,630,101-6,640,900 , GRCh37.p13 chr2: 6,770,233-6,781,032 LINC01246
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314874copy number variation1nstd102humanUncertain significance GRCh38 chr2: 6,154,935-7,419,585 , GRCh37.p13 chr2: 6,295,067-7,559,716 LOC107985845, LOC105373402, 20 more genes
    nsv6290392copy number variation1nstd102humanUncertain significance GRCh37 chr2: 6,297,801-7,555,446 , GRCh38.p12 chr2: 6,157,669-7,415,315 LOC105373404, LOC105373401, 19 more genes
    nsv5357562translocation1nstd200human GRCh38 chr2: 6,631,801-6,631,801 , GRCh38 chr2: 6,630,817-6,630,817 , GRCh37.p13 chr2: 6,771,933-6,771,933 , GRCh37.p13 chr2: 6,770,949-6,770,949 LINC01246
    nsv5339876translocation1nstd200human GRCh37 chr2: 6,770,949-6,770,949 , GRCh37 chr2: 6,771,933-6,771,933 , GRCh38.p12 chr2: 6,631,801-6,631,801 , GRCh38.p12 chr2: 6,630,817-6,630,817 LINC01246
    nsv4904734copy number variation1nstd200human GRCh38 chr2: 6,630,235-6,631,794 , GRCh37.p13 chr2: 6,770,367-6,771,926 LINC01246
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