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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099181copy number variation1nstd231human GRCh38.p12 chr1: 18,899,486-20,046,918 , GRCh37 chr1: 19,225,980-20,373,411 CAPZB, HTR6, 32 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv6646902copy number variation1nstd229human GRCh38 chr1: 19,812,811-19,820,538 , GRCh37.p13 chr1: 20,139,304-20,147,031 RNF186
    nsv6646901copy number variation1nstd229human GRCh38 chr1: 19,781,001-19,812,500 , GRCh37.p13 chr1: 20,107,494-20,138,993 RNF186, TMCO4
    nsv6646899copy number variation1nstd229human GRCh38 chr1: 19,751,232-20,412,088 , GRCh37.p13 chr1: 20,077,725-20,738,581 LOC105376826, LOC105376823, 17 more genes
    nsv6625726copy number variation1nstd224human GRCh37 chr1: 20,027,271-20,158,241 , GRCh38.p12 chr1: 19,700,778-19,831,748 RNF186, TMCO4
    nsv6333733copy number variation1nstd223human GRCh38 chr1: 19,805,902-19,813,409 , GRCh37.p13 chr1: 20,132,395-20,139,902 RNF186
    nsv6290472copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,773,001-20,221,073 , GRCh38.p12 chr1: 16,446,506-19,894,580 MIR1290, RNU6-1099P, 92 more genes
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6133962copy number variation1nstd213human GRCh37 chr1: 19,870,000-20,530,001 , GRCh38.p12 chr1: 19,543,506-20,203,508 HTR6, NBL1, 18 more genes
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 more genes
    nsv6133572copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,950,001 , GRCh38.p12 chr1: 16,943,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5285145copy number variation1nstd204human GRCh38.p13 chr1: 19,608,167-20,538,182 , GRCh37.p13 chr1: 19,934,661-20,864,675 PLA2G2C, LOC105376826, 25 more genes
    nsv5215152copy number variation1nstd204human GRCh38.p13 chr1: 19,608,201-20,098,100 , GRCh37.p13 chr1: 19,934,695-20,424,593 LOC100419911, NBL1, 12 more genes
    nsv4895177copy number variation1nstd200human GRCh38 chr1: 19,733,172-19,842,056 , GRCh37.p13 chr1: 20,059,665-20,168,549 RNF186, TMCO4
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