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Items: 1 to 20 of 248

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959013insertion1nstd209human GRCh38 chr8: 100,256,511-100,256,511 , GRCh37.p13 chr8: 101,268,739-101,268,739 RNF19A
    nsv5253073copy number variation1nstd204human GRCh38.p13 chr8: 100,267,663-100,269,363 , GRCh37.p13 chr8: 101,279,891-101,281,591 RNF19A
    nsv5106459mobile element insertion1nstd203human GRCh38 chr8: 100,318,049-100,318,065 , GRCh37.p13 chr8: 101,330,277-101,330,293 RNF19A
    nsv5104138mobile element insertion1nstd203human GRCh38 chr8: 100,271,923-100,271,936 , GRCh37.p13 chr8: 101,284,151-101,284,164 RNF19A
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4965651copy number variation1nstd200human GRCh38 chr8: 100,289,128-100,302,629 , GRCh37.p13 chr8: 101,301,356-101,314,857 RNF19A
    nsv4961515copy number variation1nstd200human GRCh38 chr8: 100,327,419-100,328,600 , GRCh37.p13 chr8: 101,339,647-101,340,828 RNF19A
    nsv4961514copy number variation1nstd200human GRCh38 chr8: 100,282,207-100,284,126 , GRCh37.p13 chr8: 101,294,435-101,296,354 RNF19A
    nsv4961513copy number variation1nstd200human GRCh38 chr8: 100,271,109-100,271,985 , GRCh37.p13 chr8: 101,283,337-101,284,213 RNF19A
    nsv4829206copy number variation1nstd200human GRCh37 chr8: 101,301,356-101,314,857 , GRCh38.p12 chr8: 100,289,128-100,302,629 RNF19A
    nsv4822636copy number variation1nstd200human GRCh37 chr8: 101,294,435-101,296,354 , GRCh38.p12 chr8: 100,282,207-100,284,126 RNF19A
    nsv4822635copy number variation1nstd200human GRCh37 chr8: 101,283,337-101,284,213 , GRCh38.p12 chr8: 100,271,109-100,271,985 RNF19A
    nsv4676096copy number variation1nstd102humanUncertain significance GRCh37 chr8: 100,791,383-101,278,033 , GRCh38.p12 chr8: 99,779,155-100,265,805 UFM1P3, COX6C, 8 more genes
    nsv4612041copy number variation1nstd183human GRCh37 chr8: 101,277,138-101,282,063 , GRCh38.p12 chr8: 100,264,910-100,269,835 RNF19A
    nsv4550723insertion1nstd166human GRCh37.p13 chr8: 101,301,483-101,301,483 , GRCh38.p12 chr8: 100,289,255-100,289,255 RNF19A
    nsv4549876insertion1nstd166human GRCh37.p13 chr8: 101,314,599-101,314,599 , GRCh38.p12 chr8: 100,302,371-100,302,371 RNF19A
    nsv4485849mobile element insertion1nstd166human GRCh37.p13 chr8: 101,276,826-101,276,826 , GRCh38.p12 chr8: 100,264,598-100,264,598 RNF19A
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
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