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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137808copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr19: 49,568,107-49,662,685 , GRCh37 chr19: 50,071,364-50,165,942 IRF3, PRRG2, 4 more genes
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5021002copy number variation1nstd200human GRCh38 chr19: 49,632,587-49,634,288 , GRCh37.p13 chr19: 50,135,844-50,137,545 RRAS
    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
    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
    nsv4271689copy number variation1nstd166human GRCh37.p13 chr19: 50,142,578-50,152,122 , GRCh38.p12 chr19: 49,639,321-49,648,865 RRAS, SCAF1
    nsv4271510copy number variation1nstd166human GRCh37.p13 chr19: 50,136,135-50,138,054 , GRCh38.p12 chr19: 49,632,878-49,634,797 RRAS
    nsv4267176copy number variation1nstd166human GRCh37.p13 chr19: 50,141,500-50,147,050 , GRCh38.p12 chr19: 49,638,243-49,643,793 RRAS, SCAF1
    nsv3963873copy number variation1nstd168human GRCh38 chr19: 49,636,703-49,666,868 , GRCh37.p13 chr19: 50,139,960-50,170,125 RRAS, BCL2L12, 2 more genes
    nsv3961459insertion1nstd168human GRCh38 chr19: 49,634,619-49,636,703 , GRCh37.p13 chr19: 50,137,876-50,139,960 RRAS
    nsv3919076copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206 KCNA7, ZNF28, 697 more genes
    nsv3911950copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965 LOC107987270, MIR6799, 694 more genes
    nsv3910302copy number variation1nstd102humanBenign NCBI36 chr19: 54,818,342-54,942,432 , GRCh38 chr19: 49,623,273-49,747,363 , GRCh37 chr19: 50,126,530-50,250,620 TSKS, CPT1C, 10 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
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