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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143797insertion1nstd232human GRCh37.p13 chr2: 19,683,051-19,683,051 , GRCh38.p12 chr2: 19,483,290-19,483,290 LINC01808
    nsv7140041insertion1nstd232human GRCh37.p13 chr2: 19,682,757-19,682,757 , GRCh38.p12 chr2: 19,482,996-19,482,996 LINC01808
    nsv7054657inversion1nstd229human GRCh38 chr2: 18,305,934-19,842,483 , GRCh37.p13 chr2: 18,487,200-20,042,244 OSR1, CISD1P1, 14 more genes
    nsv6677465copy number variation1nstd229human GRCh38 chr2: 19,483,241-19,489,869 , GRCh37.p13 chr2: 19,683,002-19,689,630 LINC01808
    nsv6664979copy number variation1nstd229human GRCh38 chr2: 19,478,960-19,482,639 , GRCh37.p13 chr2: 19,678,721-19,682,400 LINC01808
    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
    nsv6661695copy number variation1nstd229human GRCh38 chr2: 19,484,201-19,543,000 , GRCh37.p13 chr2: 19,683,962-19,742,761 LINC01808
    nsv6660744copy number variation1nstd229human GRCh38 chr2: 19,459,388-19,475,981 , GRCh37.p13 chr2: 19,659,149-19,675,742 LOC101928196, LINC01808
    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
    nsv6346197copy number variation1nstd223human GRCh38 chr2: 19,499,901-19,501,200 , GRCh37.p13 chr2: 19,699,662-19,700,961 LINC01808
    nsv6343915copy number variation1nstd223human GRCh38 chr2: 19,511,124-19,511,551 , GRCh37.p13 chr2: 19,710,885-19,711,312 LINC01808
    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
    nsv6340945copy number variation1nstd223human GRCh38 chr2: 19,416,521-20,093,799 , GRCh37.p13 chr2: 19,616,282-20,293,560 LOC105373459, LINC00954, 12 more genes
    nsv6339773copy number variation1nstd223human GRCh38 chr2: 19,483,348-20,077,709 , GRCh37.p13 chr2: 19,683,109-20,277,470 LAPTM4A, TTC32, 10 more genes
    nsv6337299copy number variation1nstd223human GRCh38 chr2: 19,478,956-19,482,639 , GRCh37.p13 chr2: 19,678,717-19,682,400 LINC01808
    nsv6336896copy number variation1nstd223human GRCh38 chr2: 19,483,239-19,489,869 , GRCh37.p13 chr2: 19,683,000-19,689,630 LINC01808
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6281513insertion1nstd214human GRCh38 chr2: 19,482,971-19,482,971 , GRCh37.p13 chr2: 19,682,732-19,682,732 LINC01808
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