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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv7017614copy number variation1nstd229human GRCh38 chr19: 49,807,211-49,854,415 , GRCh37.p13 chr19: 50,310,468-50,357,672 LOC105372435, MED25, 6 more genes
    nsv7002519copy number variation1nstd229human GRCh38 chr19: 49,765,601-49,854,600 , GRCh37.p13 chr19: 50,268,858-50,357,857 LOC105372435, MED25, 8 more genes
    nsv7001033copy number variation1nstd229human GRCh38 chr19: 49,796,501-49,923,300 , GRCh37.p13 chr19: 50,299,758-50,426,557 AP2A1, LOC105372435, 13 more genes
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6530168copy number variation1nstd223human GRCh38 chr19: 49,849,178-49,850,205 , GRCh37.p13 chr19: 50,352,435-50,353,462 PTOV1-AS1, PTOV1
    nsv6515977copy number variation1nstd223human GRCh38 chr19: 49,846,425-49,847,340 , GRCh37.p13 chr19: 50,349,682-50,350,597 PTOV1-AS1, PTOV1
    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
    nsv6310544copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,519,325-50,366,015 , GRCh38.p12 chr19: 49,016,068-49,862,758 CGB5, MED25, 76 more genes
    nsv6146782copy number variation1nstd206human GRCh38 chr19: 49,842,874-49,850,874 , GRCh37.p13 chr19: 50,346,131-50,354,131 PTOV1, PTOV1-AS1
    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
    nsv5716482mobile element insertion1nstd211human GRCh38 chr19: 49,848,035-49,848,035 , GRCh37.p13 chr19: 50,351,292-50,351,292 PTOV1-AS1, PTOV1
    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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