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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5934952copy number variation1nstd209human GRCh38 chr19: 7,640,059-7,640,324 , GRCh37.p13 chr19: 7,704,945-7,705,210 STXBP2
    nsv5653279insertion1nstd207human GRCh38 chr19: 7,644,013-7,644,013 , GRCh37.p13 chr19: 7,708,899-7,708,899 STXBP2
    nsv5558814sequence alteration1nstd206human GRCh38 chr19: 7,636,588-7,636,597 , GRCh37.p13 chr19: 7,701,474-7,701,483 STXBP2, PCP2
    nsv5326720translocation1nstd204human GRCh38.p13 chr19: 2,282,380-2,282,380 , GRCh38.p13 chr19: 7,636,598-7,636,598 , GRCh37.p13 chr19: 2,282,379-2,282,379 , GRCh37.p13 chr19: 7,701,484-7,701,484 STXBP2, PCP2, 1 more genes
    nsv5323914translocation1nstd204human GRCh38.p13 chr19: 2,282,479-2,282,479 , GRCh38.p13 chr19: 7,636,588-7,636,588 , GRCh37.p13 chr19: 2,282,478-2,282,478 , GRCh37.p13 chr19: 7,701,474-7,701,474 STXBP2, PCP2, 1 more genes
    nsv5322021copy number variation1nstd204human GRCh38.p13 chr19: 7,648,073-7,651,292 , GRCh37.p13 chr19: 7,712,959-7,716,178 STXBP2
    nsv5294732copy number variation1nstd204human GRCh38.p13 chr19: 7,648,101-7,651,300 , GRCh37.p13 chr19: 7,712,987-7,716,186 STXBP2
    nsv5285504copy number variation1nstd204human GRCh38.p13 chr19: 7,647,893-7,651,392 , GRCh37.p13 chr19: 7,712,779-7,716,278 STXBP2
    nsv5196100mobile element insertion1nstd203human GRCh38 chr19: 7,638,608-7,638,619 , GRCh37.p13 chr19: 7,703,494-7,703,505 STXBP2
    nsv5027575copy number variation1nstd200human GRCh38 chr19: 7,648,088-7,651,266 , GRCh37.p13 chr19: 7,712,974-7,716,152 STXBP2
    nsv5027574copy number variation1nstd200human GRCh38 chr19: 7,636,337-7,640,462 , GRCh37.p13 chr19: 7,701,223-7,705,348 STXBP2, PCP2
    nsv5014449copy number variation1nstd200human GRCh38 chr19: 7,617,680-7,657,475 , GRCh37.p13 chr19: 7,682,566-7,722,361 MIR6792, PCP2, 4 more genes
    nsv4852830copy number variation1nstd200human GRCh37 chr19: 7,712,974-7,716,152 , GRCh38.p12 chr19: 7,648,088-7,651,266 STXBP2
    nsv4760920insertion1nstd199human GRCh37 chr19: 7,708,898-7,708,898 , GRCh38.p12 chr19: 7,644,012-7,644,012 STXBP2
    nsv4682037copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,587,617-8,373,194 , GRCh38.p12 chr19: 7,522,731-8,308,310 XAB2, CLEC4G, 40 more genes
    nsv4676269copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,657,490-8,569,762 , GRCh38.p12 chr19: 7,592,604-8,504,878 LRRC8E, CLEC4GP1, 47 more genes
    nsv4634213copy number variation2nstd183human GRCh37 chr19: 7,704,763-7,705,305 , GRCh38.p12 chr19: 7,639,877-7,640,419 STXBP2
    nsv4629101copy number variation1nstd183human GRCh37 chr19: 7,397,015-7,925,985 , GRCh38.p12 chr19: 7,332,094-7,861,099 , PEX11G, 27 more genes
    nsv4624596copy number variation1nstd183human GRCh37 chr19: 7,704,763-7,706,068 , GRCh38.p12 chr19: 7,639,877-7,641,182 STXBP2
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