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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5975448inversion1nstd209human GRCh38 chr14: 57,580,296-59,028,517 , GRCh37.p13 chr14: 58,047,014-59,495,235 PSMA3, ARID4A, 26 more genes
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5936760copy number variation1nstd209human GRCh38 chr14: 58,340,601-58,340,735 , GRCh37.p13 chr14: 58,807,319-58,807,453 ARID4A
    nsv5278254copy number variation1nstd204human GRCh38.p13 chr14: 58,296,439-58,299,952 , GRCh37.p13 chr14: 58,763,157-58,766,670 PSMA3-AS1, ARID4A
    nsv5157610mobile element insertion1nstd203human GRCh38 chr14: 58,346,927-58,346,973 , GRCh37.p13 chr14: 58,813,645-58,813,691 ARID4A
    nsv5140183mobile element insertion1nstd203human GRCh38 chr14: 58,310,937-58,310,950 , GRCh37.p13 chr14: 58,777,655-58,777,668 ARID4A
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004658copy number variation1nstd200human GRCh38 chr14: 58,343,655-58,349,719 , GRCh37.p13 chr14: 58,810,373-58,816,437 ARID4A
    nsv4841709copy number variation1nstd200human GRCh37 chr14: 58,769,597-58,770,710 , GRCh38.p12 chr14: 58,302,879-58,303,992 ARID4A
    nsv4743888copy number variation1nstd199human GRCh37 chr14: 58,783,614-58,783,793 , GRCh38.p12 chr14: 58,316,896-58,317,075 ARID4A
    nsv4676003copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,735,449-58,853,507 , GRCh38.p12 chr14: 58,268,731-58,386,789 ARID4A, HMGB1P14, 5 more genes
    nsv4674918copy number variation1nstd102humanPathogenic GRCh37 chr14: 56,605,398-59,404,256 , GRCh38.p12 chr14: 56,138,680-58,937,538 RNU6-1204P, LOC440180, 42 more genes
    nsv4667626copy number variation1nstd186human GRCh37 chr14: 58,764,774-58,765,247 , GRCh38.p12 chr14: 58,298,056-58,298,529 ARID4A, PSMA3-AS1
    nsv4632051copy number variation1nstd183human GRCh37 chr14: 58,839,313-58,840,062 , GRCh38.p12 chr14: 58,372,595-58,373,344 ARID4A, TOMM20L-DT
    nsv4626127copy number variation2nstd183human GRCh37 chr14: 58,764,774-58,765,247 , GRCh38.p12 chr14: 58,298,056-58,298,529 PSMA3-AS1, ARID4A
    nsv4619085copy number variation1nstd183human GRCh37 chr14: 58,839,313-58,843,879 , GRCh38.p12 chr14: 58,372,595-58,377,161 ARID4A, TOMM20L-DT
    nsv4548276insertion1nstd166human GRCh37.p13 chr14: 58,815,559-58,815,559 , GRCh38.p12 chr14: 58,348,841-58,348,841 ARID4A
    nsv4530423copy number variation1nstd166human GRCh37.p13 chr14: 58,816,072-58,816,817 , GRCh38.p12 chr14: 58,349,354-58,350,099 ARID4A
    nsv4510516mobile element insertion1nstd166human GRCh37.p13 chr14: 58,777,655-58,777,655 , GRCh38.p12 chr14: 58,310,937-58,310,937 ARID4A
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