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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095288copy number variation1nstd102humanPathogenic GRCh37 chr19: 51,727,962-51,890,697 , GRCh38.p12 chr19: 51,224,706-51,387,443 LOC107985327, LIM2-AS1, 13 more genes
    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
    nsv7062200inversion1nstd229human GRCh38 chr19: 51,156,828-51,481,685 , GRCh37.p13 chr19: 51,660,085-51,984,939 VSIG10L, SIGLEC20P, 27 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
    nsv6291759copy number variation1nstd102humanUncertain significance GRCh37 chr19: 51,769,834-52,415,762 , GRCh38.p12 chr19: 51,266,580-51,912,509 ZNF649-AS1, SIGLEC12, 46 more genes
    nsv6251109mobile element insertion1nstd215human GRCh38 chr19: 51,266,114-51,266,114 , GRCh37.p13 chr19: 51,769,368-51,769,368 SIGLECL1, LOC107985327
    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
    nsv5329338copy number variation1nstd204human GRCh37.p13 chr19: 51,764,707-51,766,783 , GRCh38.p13 chr19: 51,261,453-51,263,529 LOC107985327, SIGLECL1
    nsv5170533mobile element insertion1nstd203human GRCh38 chr19: 51,261,957-51,261,972 , GRCh37.p13 chr19: 51,765,211-51,765,226 SIGLECL1, LOC107985327
    nsv5169964mobile element insertion1nstd203human GRCh38 chr19: 51,269,013-51,269,027 , GRCh37.p13 chr19: 51,772,267-51,772,281 SIGLECL1, LOC107985327
    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
    nsv4629371copy number variation1nstd183human GRCh37 chr19: 51,751,123-51,772,194 , GRCh38.p12 chr19: 51,247,868-51,268,940 SIGLECL1, LOC107985327
    nsv4261234copy number variation1nstd166human GRCh37.p13 chr19: 51,754,132-51,754,216 , GRCh38.p12 chr19: 51,250,878-51,250,962 SIGLECL1, LOC107985327
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