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Items: 1 to 20 of 96

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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
    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
    nsv5933561copy number variation1nstd209human GRCh38 chr19: 50,847,831-50,853,147 , GRCh37.p13 chr19: 51,351,087-51,356,403 KLK3, LOC105372441
    nsv5705917mobile element insertion1nstd211human GRCh38 chr19: 50,860,289-50,860,289 , GRCh37.p13 chr19: 51,363,545-51,363,545 KLK3
    nsv5527745copy number variation1nstd206human GRCh38 chr19: 50,847,831-50,853,117 , GRCh37.p13 chr19: 51,351,087-51,356,373 LOC105372441, KLK3
    nsv5428826mobile element insertion1nstd206human GRCh38 chr19: 50,860,289-50,860,340 , GRCh37.p13 chr19: 51,363,545-51,363,596 KLK3
    nsv5359895translocation1nstd200human GRCh38 chr19: 50,855,902-50,855,902 , GRCh38 chr19: 50,855,372-50,855,372 , GRCh37.p13 chr19: 51,359,158-51,359,158 , GRCh37.p13 chr19: 51,358,628-51,358,628 KLK3
    nsv5021076copy number variation1nstd200human GRCh38 chr19: 50,859,425-50,877,811 , GRCh37.p13 chr19: 51,362,681-51,381,067 KLK3, KLK2
    nsv4853410copy number variation1nstd200human GRCh37 chr19: 51,362,699-51,381,042 , GRCh38.p12 chr19: 50,859,443-50,877,786 KLK3, KLK2
    nsv4853409copy number variation1nstd200human GRCh37 chr19: 51,358,628-51,359,158 , GRCh38.p12 chr19: 50,855,372-50,855,902 KLK3
    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
    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
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