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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5872305copy number variation1nstd209human GRCh38 chr19: 49,890,440-49,891,576 , GRCh37.p13 chr19: 50,393,697-50,394,833 IL4I1
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5528422copy number variation1nstd206human GRCh38 chr19: 49,898,817-49,903,146 , GRCh37.p13 chr19: 50,402,074-50,406,403 IL4I1
    nsv5522261copy number variation1nstd206human GRCh38 chr19: 49,904,460-49,904,765 , GRCh37.p13 chr19: 50,407,717-50,408,022 IL4I1
    nsv5516385copy number variation1nstd206human GRCh38 chr19: 49,863,321-50,035,426 , GRCh37.p13 chr19: 50,366,578-50,538,683 IL4I1, SIGLEC11, 10 more genes
    nsv5322461copy number variation1nstd204human GRCh38.p13 chr19: 49,904,434-49,904,790 , GRCh37.p13 chr19: 50,407,691-50,408,047 IL4I1
    nsv5024818copy number variation1nstd200human GRCh38 chr19: 49,898,734-49,903,096 , GRCh37.p13 chr19: 50,401,991-50,406,353 IL4I1
    nsv5024817copy number variation1nstd200human GRCh38 chr19: 49,856,044-49,921,115 , GRCh37.p13 chr19: 50,359,301-50,424,372 IL4I1, AKT1S1, 6 more genes
    nsv5021013copy number variation1nstd200human GRCh38 chr19: 49,904,979-49,906,475 , GRCh37.p13 chr19: 50,408,236-50,409,732 IL4I1, NUP62
    nsv5021012copy number variation1nstd200human GRCh38 chr19: 49,893,710-49,894,389 , GRCh37.p13 chr19: 50,396,967-50,397,646 IL4I1
    nsv4865264copy number variation1nstd200human GRCh37 chr19: 50,401,982-50,406,371 , GRCh38.p12 chr19: 49,898,725-49,903,114 IL4I1
    nsv4853351copy number variation1nstd200human GRCh37 chr19: 50,416,129-50,416,468 , GRCh38.p12 chr19: 49,912,872-49,913,211 NUP62, IL4I1
    nsv4853350copy number variation1nstd200human GRCh37 chr19: 50,408,255-50,409,704 , GRCh38.p12 chr19: 49,904,998-49,906,447 IL4I1, NUP62
    nsv4853349copy number variation1nstd200human GRCh37 chr19: 50,396,967-50,397,646 , GRCh38.p12 chr19: 49,893,710-49,894,389 IL4I1
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4627115copy number variation1nstd183human GRCh37 chr19: 50,427,995-50,504,630 , GRCh38.p12 chr19: 49,924,738-50,001,373 ATF5, NUP62, 5 more genes
    nsv4514090mobile element insertion1nstd166human GRCh37.p13 chr19: 50,425,638-50,425,638 , GRCh38.p12 chr19: 49,922,381-49,922,381 NUP62, IL4I1
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