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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv5952832insertion1nstd209human GRCh38 chr4: 22,785,573-22,785,573 , GRCh37.p13 chr4: 22,787,196-22,787,196 GBA3
    nsv5907498copy number variation1nstd209human GRCh38 chr4: 22,730,142-22,731,337 , GRCh37.p13 chr4: 22,731,765-22,732,960 LOC105374521, GBA3
    nsv5900364copy number variation1nstd209human GRCh38 chr4: 22,726,483-22,726,544 , GRCh37.p13 chr4: 22,728,106-22,728,167 , GBA3, 1 more genes
    nsv5893786copy number variation1nstd209human GRCh38 chr4: 22,778,369-22,778,484 , GRCh37.p13 chr4: 22,779,992-22,780,107 GBA3
    nsv5838903copy number variation1nstd209human GRCh38 chr4: 22,730,154-22,731,353 , GRCh37.p13 chr4: 22,731,777-22,732,976 LOC105374521, GBA3
    nsv5729393mobile element insertion1nstd211human GRCh38 chr4: 22,710,701-22,710,701 , GRCh37.p13 chr4: 22,712,324-22,712,324 GBA3
    nsv5728776mobile element insertion1nstd211human GRCh38 chr4: 22,719,376-22,719,376 , GRCh37.p13 chr4: 22,720,999-22,720,999 GBA3
    nsv5575586copy number variation1nstd207human GRCh38 chr4: 22,726,462-22,726,523 , GRCh37.p13 chr4: 22,728,085-22,728,146 , GBA3, 1 more genes
    nsv5563071sequence alteration1nstd206human GRCh38 chr4: 22,590,995-23,538,734 , GRCh37.p13 chr4: 22,592,618-23,540,357 , GBA3, 7 more genes
    nsv5448261copy number variation1nstd206human GRCh38 chr4: 22,724,768-22,726,362 , GRCh37.p13 chr4: 22,726,391-22,727,985 , GBA3, 1 more genes
    nsv5444229copy number variation1nstd206human GRCh38 chr4: 22,699,132-22,775,478 , GRCh37.p13 chr4: 22,700,755-22,777,101 , GBA3, 2 more genes
    nsv5442045copy number variation1nstd206human GRCh38 chr4: 22,778,392-22,778,445 , GRCh37.p13 chr4: 22,780,015-22,780,068 GBA3
    nsv5437900copy number variation1nstd206human GRCh38 chr4: 22,766,795-22,766,898 , GRCh37.p13 chr4: 22,768,418-22,768,521 GBA3
    nsv5435123copy number variation1nstd206human GRCh38 chr4: 22,720,662-22,726,593 , GRCh37.p13 chr4: 22,722,285-22,728,216 , CDC42P6, 1 more genes
    nsv5367406translocation1nstd200human GRCh38 chr4: 22,808,239-22,808,239 , GRCh38 chr15: 88,940,176-88,940,176 , GRCh37.p13 chr15: 89,483,407-89,483,407 , GRCh37.p13 chr4: 22,809,862-22,809,862 GBA3
    nsv5352652translocation1nstd200human GRCh38 chr4: 22,793,932-22,793,932 , GRCh38 chr4: 22,793,867-22,793,867 , GRCh37.p13 chr4: 22,795,490-22,795,490 , GRCh37.p13 chr4: 22,795,555-22,795,555 GBA3
    nsv5352651translocation1nstd200human GRCh38 chr4: 22,742,421-22,742,421 , GRCh38 chr4: 22,742,363-22,742,363 , GRCh37.p13 chr4: 22,743,986-22,743,986 , GRCh37.p13 chr4: 22,744,044-22,744,044 GBA3, LOC105374521
    nsv5333069translocation1nstd200human GRCh37 chr4: 22,795,555-22,795,555 , GRCh37 chr4: 22,795,490-22,795,490 , GRCh38.p12 chr4: 22,793,867-22,793,867 , GRCh38.p12 chr4: 22,793,932-22,793,932 GBA3
    nsv5232139copy number variation1nstd204human GRCh37.p13 chr4: 22,592,324-23,172,523 , GRCh38.p13 chr4: 22,590,701-23,170,900 , GBA3, 5 more genes
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