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Items: 1 to 20 of 105

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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
    nsv5716482mobile element insertion1nstd211human GRCh38 chr19: 49,848,035-49,848,035 , GRCh37.p13 chr19: 50,351,292-50,351,292 PTOV1-AS1, PTOV1
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5520282copy number variation1nstd206human GRCh38 chr19: 49,851,253-49,851,315 , GRCh37.p13 chr19: 50,354,510-50,354,572 PTOV1, PTOV1-AS1
    nsv5320541copy number variation1nstd204human GRCh37.p13 chr19: 50,344,192-50,351,395 , GRCh38.p13 chr19: 49,840,935-49,848,138 PTOV1-AS1, PTOV1
    nsv5290722copy number variation1nstd204human GRCh38.p13 chr19: 49,836,585-49,838,684 , GRCh37.p13 chr19: 50,339,842-50,341,941 MED25, PTOV1-AS1
    nsv5284655copy number variation1nstd204human GRCh38.p13 chr19: 49,841,501-49,847,900 , GRCh37.p13 chr19: 50,344,758-50,351,157 PTOV1, PTOV1-AS1
    nsv4853346copy number variation1nstd200human GRCh37 chr19: 50,354,510-50,354,572 , GRCh38.p12 chr19: 49,851,253-49,851,315 PTOV1, PTOV1-AS1
    nsv4853345copy number variation1nstd200human GRCh37 chr19: 50,344,196-50,351,393 , GRCh38.p12 chr19: 49,840,939-49,848,136 PTOV1-AS1, PTOV1
    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
    nsv4668667copy number variation1nstd186human GRCh37 chr19: 50,354,888-50,354,934 , GRCh38.p12 chr19: 49,851,631-49,851,677 PTOV1, PTOV1-AS1
    nsv4632581copy number variation1nstd183human GRCh37 chr19: 50,354,839-50,354,934 , GRCh38.p12 chr19: 49,851,582-49,851,677 PTOV1-AS1, PTOV1
    nsv4627059copy number variation1nstd183human GRCh37 chr19: 50,354,626-50,354,934 , GRCh38.p12 chr19: 49,851,369-49,851,677 PTOV1, PTOV1-AS1
    nsv4625365copy number variation1nstd183human GRCh37 chr19: 50,354,224-50,354,934 , GRCh38.p12 chr19: 49,850,967-49,851,677 PTOV1, PTOV1-AS1
    nsv4622732copy number variation1nstd183human GRCh37 chr19: 50,354,888-50,354,934 , GRCh38.p12 chr19: 49,851,631-49,851,677 PTOV1-AS1, PTOV1
    nsv4457465copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,600,909-51,366,070 , GRCh38.p12 chr19: 49,097,652-50,862,814 MED25, EMC10, 117 more genes
    nsv4376838copy number variation1nstd173human GRCh37 chr19: 48,462,617-51,107,899 , GRCh38.p12 chr19: 47,959,360-50,604,642 , LIN7B, 173 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
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