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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095218copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,411,496-50,766,697 , GRCh38.p12 chr19: 49,908,239-50,263,440 SNAR-A6, SNAR-A14, 23 more genes
    nsv7076411inversion1nstd229human GRCh38 chr19: 49,950,371-49,971,789 , GRCh37.p13 chr19: 50,453,628-50,475,046 SIGLEC16, SIGLEC11
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 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
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7068520inversion1nstd229human GRCh38 chr19: 49,914,473-49,969,940 , GRCh37.p13 chr19: 50,417,730-50,473,197 NUP62, SIGLEC16, 4 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
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 more genes
    nsv7013373copy number variation1nstd229human GRCh38 chr19: 49,962,038-50,073,196 , GRCh37.p13 chr19: 50,465,295-50,576,453 VRK3, LOC100287477, 3 more genes
    nsv7011752copy number variation1nstd229human GRCh38 chr19: 49,968,371-49,972,103 , GRCh37.p13 chr19: 50,471,628-50,475,360 SIGLEC16
    nsv7007068copy number variation1nstd229human GRCh38 chr19: 49,955,377-49,969,479 , GRCh37.p13 chr19: 50,458,634-50,472,736 SIGLEC16, SIGLEC11
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6522417copy number variation1nstd223human GRCh38 chr19: 49,955,376-49,969,478 , GRCh37.p13 chr19: 50,458,633-50,472,735 SIGLEC16, SIGLEC11
    nsv6314099copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,355,646-50,552,140 , GRCh38.p12 chr19: 49,852,389-50,048,883 IL4I1, SIGLEC11, 14 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
    nsv6110571inversion1nstd212human GRCh38 chr19: 47,903,487-50,091,196 , GRCh37.p13 chr19: 48,406,744-50,594,453 , AP2A1, 155 more genes
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5969250inversion1nstd209human GRCh38 chr19: 49,972,119-49,985,651 , GRCh37.p13 chr19: 50,475,376-50,488,908 VRK3, SIGLEC16
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
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