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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942628copy number variation1nstd209human GRCh38 chr19: 40,459,048-40,459,181 , GRCh37.p13 chr19: 40,964,955-40,965,088 BLVRB
    nsv5940341copy number variation1nstd209human GRCh38 chr19: 40,456,380-40,457,129 , GRCh37.p13 chr19: 40,962,287-40,963,036 BLVRB
    nsv5532629copy number variation1nstd206human GRCh38 chr19: 40,451,219-40,462,584 , GRCh37.p13 chr19: 40,957,126-40,968,491 BLVRB
    nsv5532150copy number variation1nstd206human GRCh38 chr19: 40,462,259-40,465,021 , GRCh37.p13 chr19: 40,968,166-40,970,928 SPTBN4, BLVRB
    nsv5519838copy number variation1nstd206human GRCh38 chr19: 40,447,112-40,449,269 , GRCh37.p13 chr19: 40,953,019-40,955,176 BLVRB
    nsv5518398copy number variation1nstd206human GRCh38 chr19: 40,447,657-40,453,024 , GRCh37.p13 chr19: 40,953,564-40,958,931 BLVRB
    nsv5287129copy number variation1nstd204human GRCh38.p13 chr19: 40,119,401-40,793,500 , GRCh37.p13 chr19: 40,625,308-41,299,405 CCNP, SHKBP1, 28 more genes
    nsv5027998copy number variation1nstd200human GRCh38 chr19: 40,462,259-40,465,021 , GRCh37.p13 chr19: 40,968,166-40,970,928 BLVRB, SPTBN4
    nsv5027997copy number variation1nstd200human GRCh38 chr19: 40,445,359-40,450,229 , GRCh37.p13 chr19: 40,951,266-40,956,136 BLVRB, SERTAD3-AS1
    nsv5027996copy number variation1nstd200human GRCh38 chr19: 40,436,974-40,449,405 , GRCh37.p13 chr19: 40,942,881-40,955,312 BLVRB, SERTAD3-AS1, 1 more genes
    nsv5024638copy number variation1nstd200human GRCh38 chr19: 40,451,239-40,462,564 , GRCh37.p13 chr19: 40,957,146-40,968,471 BLVRB
    nsv4868375copy number variation1nstd200human GRCh37 chr19: 40,968,166-40,970,928 , GRCh38.p12 chr19: 40,462,259-40,465,021 BLVRB, SPTBN4
    nsv4868373copy number variation1nstd200human GRCh37 chr19: 40,942,881-40,955,312 , GRCh38.p12 chr19: 40,436,974-40,449,405 BLVRB, SERTAD3-AS1, 1 more genes
    nsv4865173copy number variation1nstd200human GRCh37 chr19: 40,957,146-40,968,471 , GRCh38.p12 chr19: 40,451,239-40,462,564 BLVRB
    nsv4707001copy number variation1nstd195human GRCh37 chr19: 40,971,331-40,971,332 , GRCh38.p12 chr19: 40,465,424-40,465,425 BLVRB, SPTBN4
    nsv4666137copy number variation1nstd186human GRCh37 chr19: 40,952,965-40,955,160 , GRCh38.p12 chr19: 40,447,058-40,449,253 BLVRB
    nsv4621182copy number variation1nstd183human GRCh37 chr19: 40,952,965-40,955,160 , GRCh38.p12 chr19: 40,447,058-40,449,253 BLVRB
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4263377copy number variation1nstd166human GRCh37.p13 chr19: 40,963,351-40,963,528 , GRCh38.p12 chr19: 40,457,444-40,457,621 BLVRB
    nsv4262065copy number variation1nstd166human GRCh37.p13 chr19: 40,947,000-40,952,000 , GRCh38.p12 chr19: 40,441,093-40,446,093 BLVRB, SERTAD3, 1 more genes
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