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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054657inversion1nstd229human GRCh38 chr2: 18,305,934-19,842,483 , GRCh37.p13 chr2: 18,487,200-20,042,244 OSR1, CISD1P1, 14 more genes
    nsv6674203copy number variation1nstd229human GRCh38 chr2: 19,349,168-19,350,311 , GRCh37.p13 chr2: 19,548,929-19,550,072 OSR1
    nsv6663705copy number variation1nstd229human GRCh38 chr2: 19,200,219-20,084,308 , GRCh37.p13 chr2: 19,399,980-20,284,069 WDR35-DT, LOC105373458, 14 more genes
    nsv6661928copy number variation1nstd229human GRCh38 chr2: 19,355,841-19,355,935 , GRCh37.p13 chr2: 19,555,602-19,555,696 OSR1
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6352960copy number variation1nstd223human GRCh38 chr2: 19,163,946-19,538,550 , GRCh37.p13 chr2: 19,363,707-19,738,311 LOC101928196, LOC105373458, 3 more genes
    nsv6342128copy number variation1nstd223human GRCh38 chr2: 19,200,219-20,084,308 , GRCh37.p13 chr2: 19,399,980-20,284,069 LAPTM4A-DT, LINC01808, 14 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6112733copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,640,273-19,609,496 , GRCh38.p12 chr2: 15,500,149-19,409,735 LOC112267888, LOC105373454, 40 more genes
    nsv5435530copy number variation1nstd206human GRCh38 chr2: 19,352,035-19,352,086 , GRCh37.p13 chr2: 19,551,796-19,551,847 OSR1
    nsv4728515copy number variation1nstd102humanUncertain significance GRCh37 chr2: 19,368,077-19,743,086 , GRCh38.p12 chr2: 19,168,316-19,543,325 MIR4757, LINC01808, 3 more genes
    nsv4585048copy number variation1nstd183human GRCh37 chr2: 19,469,262-19,696,376 , GRCh38.p12 chr2: 19,269,501-19,496,615 LOC101928196, LOC105373458, 3 more genes
    nsv4451022copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621 RAD51AP2, LOC101928149, 82 more genes
    nsv4366611copy number variation1nstd173human GRCh37 chr2: 19,473,126-19,696,375 , GRCh38.p12 chr2: 19,273,365-19,496,614 LOC101928196, LINC01808, 3 more genes
    nsv4071695copy number variation1nstd166human GRCh37.p13 chr2: 19,548,928-19,550,071 , GRCh38.p12 chr2: 19,349,167-19,350,310 OSR1
    nsv3961768copy number variation1nstd168human GRCh38 chr2: 19,327,112-19,388,450 , GRCh37.p13 chr2: 19,526,873-19,588,211 OSR1, MIR4757
    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
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