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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077997inversion1nstd229human GRCh38 chr19: 50,085,764-53,270,581 , GRCh37.p13 chr19: 50,589,021-53,773,834 SNORD88B, ZNF320, 181 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7069681inversion1nstd229human GRCh38 chr19: 50,654,313-52,443,676 , GRCh37.p13 chr19: 51,157,570-52,946,929 CTU1, LOC100419835, 117 more genes
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 more genes
    nsv7008886copy number variation1nstd229human GRCh38 chr19: 51,153,284-51,154,690 , GRCh37.p13 chr19: 51,656,541-51,657,947 LOC101928517, SIGLEC7
    nsv6637793copy number variation1nstd102humanUncertain significance GRCh37 chr19: 51,623,330-51,694,022 , GRCh38.p12 chr19: 51,120,073-51,190,766 SIGLEC9, SIGLEC20P, 4 more genes
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5021095copy number variation1nstd200human GRCh38 chr19: 51,124,736-51,142,082 , GRCh37.p13 chr19: 51,627,993-51,645,339 SIGLEC7, SIGLEC9
    nsv4853429copy number variation1nstd200human GRCh37 chr19: 51,648,912-51,649,013 , GRCh38.p12 chr19: 51,145,655-51,145,756 SIGLEC7
    nsv4853428copy number variation1nstd200human GRCh37 chr19: 51,627,993-51,645,339 , GRCh38.p12 chr19: 51,124,736-51,142,082 SIGLEC9, SIGLEC7
    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
    nsv4676347copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,469,730-51,916,485 , GRCh38.p12 chr19: 49,966,473-51,413,231 VRK3, SYT3, 93 more genes
    nsv4373874copy number variation1nstd173human GRCh37 chr19: 51,625,682-51,676,680 , GRCh38.p12 chr19: 51,122,425-51,173,423 SIGLEC7, SIGLEC9, 2 more genes
    nsv4271766copy number variation1nstd166human GRCh37.p13 chr19: 51,637,460-51,686,628 , GRCh38.p12 chr19: 51,134,203-51,183,372 SIGLEC7, SIGLEC17P, 3 more genes
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 RPL39P37, CCDC106, 556 more genes
    nsv3923909copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203 OSCAR, FKBP1AP1, 535 more genes
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