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Items: 1 to 20 of 385

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5906787copy number variation1nstd209human GRCh38 chr3: 125,993,401-126,003,225 , GRCh37.p13 chr3: 125,712,244-125,722,068 ALG1L1P
    nsv5897310copy number variation1nstd209human GRCh38 chr3: 125,928,901-125,928,952 , GRCh37.p13 chr3: 125,647,744-125,647,795 ALG1L1P, FAM86JP
    nsv5894705copy number variation1nstd209human GRCh38 chr3: 125,961,846-125,961,944 , GRCh37.p13 chr3: 125,680,689-125,680,787 ALG1L1P
    nsv5891433copy number variation1nstd209human GRCh38 chr3: 125,953,468-125,957,532 , GRCh37.p13 chr3: 125,672,311-125,676,375 ALG1L1P, FBRSL1P1
    nsv5834886copy number variation1nstd209human GRCh38 chr3: 125,993,380-126,003,267 , GRCh37.p13 chr3: 125,712,223-125,722,110 ALG1L1P
    nsv5834578copy number variation1nstd209human GRCh38 chr3: 125,953,405-125,957,510 , GRCh37.p13 chr3: 125,672,248-125,676,353 ALG1L1P, FBRSL1P1
    nsv5726752mobile element insertion1nstd211human GRCh38 chr3: 125,958,082-125,958,082 , GRCh37.p13 chr3: 125,676,925-125,676,925 ALG1L1P, FBRSL1P1
    nsv5722512mobile element insertion1nstd211human GRCh38 chr3: 125,952,755-125,952,755 , GRCh37.p13 chr3: 125,671,598-125,671,598 ALG1L1P
    nsv5616348insertion1nstd207human GRCh38 chr3: 125,995,825-125,995,825 , GRCh37.p13 chr3: 125,714,668-125,714,668 ALG1L1P
    nsv5605163insertion1nstd207human GRCh38 chr3: 125,961,846-125,961,846 , GRCh37.p13 chr3: 125,680,689-125,680,689 ALG1L1P
    nsv5576851copy number variation1nstd207human GRCh38 chr3: 125,956,893-125,957,808 , GRCh37.p13 chr3: 125,675,736-125,676,651 FBRSL1P1, ALG1L1P
    nsv5575384copy number variation1nstd207human GRCh38 chr3: 125,957,971-125,961,622 , GRCh37.p13 chr3: 125,676,814-125,680,465 FBRSL1P1, ALG1L1P
    nsv5569741copy number variation1nstd207human GRCh38 chr3: 125,993,407-126,003,225 , GRCh37.p13 chr3: 125,712,250-125,722,068 ALG1L1P
    nsv5568668copy number variation1nstd207human GRCh38 chr3: 125,953,468-125,957,532 , GRCh37.p13 chr3: 125,672,311-125,676,375 FBRSL1P1, ALG1L1P
    nsv5559873inversion1nstd206human GRCh38 chr3: 125,966,603-125,980,782 , GRCh37.p13 chr3: 125,685,446-125,699,625 ROPN1B, ALG1L1P
    nsv5451457copy number variation1nstd206human GRCh38 chr3: 125,953,138-125,957,533 , GRCh37.p13 chr3: 125,671,981-125,676,376 ALG1L1P, FBRSL1P1
    nsv5444702copy number variation1nstd206human GRCh38 chr3: 125,961,846-125,961,945 , GRCh37.p13 chr3: 125,680,689-125,680,788 ALG1L1P
    nsv5439132copy number variation1nstd206human GRCh38 chr3: 125,993,401-126,003,226 , GRCh37.p13 chr3: 125,712,244-125,722,069 ALG1L1P
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