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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5879514copy number variation1nstd209human GRCh38 chr2: 11,665,407-11,665,513 , GRCh37.p13 chr2: 11,805,533-11,805,639 NTSR2, CDK8P1
    nsv5446079copy number variation1nstd206human GRCh38 chr2: 11,659,938-11,659,988 , GRCh37.p13 chr2: 11,800,064-11,800,114 NTSR2
    nsv5443087copy number variation1nstd206human GRCh38 chr2: 11,665,407-11,665,514 , GRCh37.p13 chr2: 11,805,533-11,805,640 NTSR2, CDK8P1
    nsv5435700copy number variation1nstd206human GRCh38 chr2: 11,664,722-11,664,803 , GRCh37.p13 chr2: 11,804,848-11,804,929 CDK8P1, NTSR2
    nsv4900246copy number variation1nstd200human GRCh38 chr2: 11,654,428-11,662,706 , GRCh37.p13 chr2: 11,794,554-11,802,832 NTSR2
    nsv4900245copy number variation1nstd200human GRCh38 chr2: 11,654,571-11,656,195 , GRCh37.p13 chr2: 11,794,697-11,796,321 NTSR2
    nsv4775475copy number variation1nstd200human GRCh37 chr2: 11,794,697-11,796,321 , GRCh38.p12 chr2: 11,654,571-11,656,195 NTSR2
    nsv4728305copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,144,226-12,569,011 , GRCh38.p12 chr2: 11,004,100-12,428,885 RNA5SP85, TRG-CCC7-1, 30 more genes
    nsv4674709copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,698,868-13,261,503 , GRCh38.p12 chr2: 11,558,742-13,121,378 MIR3125, LOC105373431, 23 more genes
    nsv4518570copy number variation1nstd166human GRCh37.p13 chr2: 11,408,186-12,063,773 , GRCh38.p12 chr2: 11,268,060-11,923,647 MIR548S, E2F6, 19 more genes
    nsv4455010copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,405,245-12,054,698 , GRCh38.p12 chr2: 11,265,119-11,914,572 PPIAP60, MIR4429, 19 more genes
    nsv4453469copy number variation2nstd102humanUncertain significance GRCh37 chr2: 11,410,614-12,054,698 , GRCh38.p12 chr2: 11,270,488-11,914,572 NTSR2, LOC101929752, 19 more genes
    nsv4063543copy number variation1nstd166human GRCh37.p13 chr2: 11,805,533-11,805,640 , GRCh38.p12 chr2: 11,665,407-11,665,514 CDK8P1, NTSR2
    nsv4056964copy number variation1nstd166human GRCh37.p13 chr2: 11,794,900-11,803,000 , GRCh38.p12 chr2: 11,654,774-11,662,874 NTSR2
    nsv3908896copy number variation1nstd102humanPathogenic GRCh37 chr2: 6,671,304-16,243,921 , GRCh38 chr2: 6,531,172-16,103,799 , NCBI36 chr2: 6,588,755-16,161,372 RNU6-1288P, MIR7515HG, 138 more genes
    nsv3908628copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,342-14,924,526 , GRCh37 chr2: 30,342-15,007,075 , GRCh38 chr2: 30,342-14,866,951 RPS7, RPL30P3, 198 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SLC35F6, LOC105374458, 801 more genes
    nsv3908459copy number variation1nstd102humanPathogenic NCBI36 chr2: 1,647,394-23,740,517 , GRCh38 chr2: 1,664,615-23,664,142 , GRCh37 chr2: 1,668,387-23,887,012 EIF1P7, LOC105373398, 277 more genes
    nsv3908405copy number variation1nstd102humanPathogenic GRCh38 chr2: 17,019-20,001,056 , NCBI36 chr2: 7,019-20,064,298 , GRCh37 chr2: 17,019-20,200,817 LOC100996549, LOC105373479, 252 more genes
    nsv3908288copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875 ALLC, LOC105373429, 674 more genes
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