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Items: 1 to 20 of 89

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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
    nsv7006634copy number variation1nstd229human GRCh38 chr19: 51,028,377-51,032,449 , GRCh37.p13 chr19: 51,531,633-51,535,705 KLK11, KLK12
    nsv6534752copy number variation1nstd223human GRCh38 chr19: 51,023,416-51,038,767 , GRCh37.p13 chr19: 51,526,672-51,542,024 KLK11, KLK12
    nsv6533726copy number variation1nstd223human GRCh38 chr19: 51,018,633-51,020,823 , GRCh37.p13 chr19: 51,521,889-51,524,079 KLK10, KLK11
    nsv6525605copy number variation1nstd223human GRCh38 chr19: 50,942,995-51,022,105 , GRCh37.p13 chr19: 51,446,251-51,525,361 KLK11, KLK8, 6 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
    nsv5288933copy number variation1nstd204human GRCh38.p13 chr19: 51,027,457-51,032,196 , GRCh37.p13 chr19: 51,530,713-51,535,452 KLK11, KLK12
    nsv5024833copy number variation1nstd200human GRCh38 chr19: 50,948,824-51,065,442 , GRCh37.p13 chr19: 51,452,080-51,568,699 , KLK11, 9 more genes
    nsv5021089copy number variation1nstd200human GRCh38 chr19: 51,020,803-51,021,926 , GRCh37.p13 chr19: 51,524,059-51,525,182 KLK11
    nsv5021088copy number variation1nstd200human GRCh38 chr19: 51,018,637-51,020,843 , GRCh37.p13 chr19: 51,521,893-51,524,099 KLK11, KLK10
    nsv4865271copy number variation1nstd200human GRCh37 chr19: 51,452,080-51,568,699 , GRCh38.p12 chr19: 50,948,824-51,065,442 , KLK12, 9 more genes
    nsv4853420copy number variation1nstd200human GRCh37 chr19: 51,524,059-51,525,182 , GRCh38.p12 chr19: 51,020,803-51,021,926 KLK11
    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
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