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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 PHF7, SEMA3G, 47 more genes
    nsv7096957copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,018,081-52,188,388 , GRCh38.p12 chr3: 51,984,065-52,154,372 ACY1, DUSP7, 5 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv7050795inversion1nstd229human GRCh38 chr3: 52,147,285-52,147,405 , GRCh37.p13 chr3: 52,181,301-52,181,421 POC1A
    nsv6717409copy number variation1nstd229human GRCh38 chr3: 52,096,401-52,099,600 , GRCh37.p13 chr3: 52,130,417-52,133,616 POC1A
    nsv6715936copy number variation1nstd229human GRCh38 chr3: 52,090,708-52,095,057 , GRCh37.p13 chr3: 52,124,724-52,129,073 POC1A
    nsv6712933copy number variation1nstd229human GRCh38 chr3: 52,152,075-52,152,211 , GRCh37.p13 chr3: 52,186,091-52,186,227 POC1A
    nsv6711686copy number variation1nstd229human GRCh38 chr3: 51,850,901-52,533,900 , GRCh37.p13 chr3: 51,884,917-52,567,916 LOC105377088, GLYCTK-AS1, 37 more genes
    nsv6708778copy number variation1nstd229human GRCh38 chr3: 52,071,015-52,133,314 , GRCh37.p13 chr3: 52,105,031-52,167,330 POC1A
    nsv6707028copy number variation1nstd229human GRCh38 chr3: 52,154,799-52,154,830 , GRCh37.p13 chr3: 52,188,815-52,188,846 POC1A
    nsv6704681copy number variation1nstd229human GRCh38 chr3: 52,080,488-52,080,845 , GRCh37.p13 chr3: 52,114,504-52,114,861 POC1A
    nsv6704351copy number variation1nstd229human GRCh38 chr3: 52,065,520-52,074,128 , GRCh37.p13 chr3: 52,099,536-52,108,144 POC1A, LINC00696
    nsv6700952copy number variation1nstd229human GRCh38 chr3: 52,099,792-52,105,080 , GRCh37.p13 chr3: 52,133,808-52,139,096 POC1A
    nsv6698351copy number variation1nstd229human GRCh38 chr3: 52,078,973-52,085,985 , GRCh37.p13 chr3: 52,112,989-52,120,001 POC1A
    nsv6543472inversion1nstd223human GRCh38 chr3: 52,119,276-52,123,984 , GRCh37.p13 chr3: 52,153,292-52,158,000 POC1A
    nsv6361118copy number variation1nstd223human GRCh38 chr3: 52,090,701-52,095,300 , GRCh37.p13 chr3: 52,124,717-52,129,316 POC1A
    nsv6311880copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,172,193-52,212,093 , GRCh38.p12 chr3: 52,138,177-52,178,077 POC1A
    nsv6254012mobile element insertion1nstd215human GRCh38 chr3: 52,135,986-52,135,986 , GRCh37.p13 chr3: 52,170,002-52,170,002 POC1A
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
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