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Items: 1 to 20 of 154

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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
    nsv5973419inversion1nstd209human GRCh38 chr14: 55,370,706-55,523,196 , GRCh37.p13 chr14: 55,837,424-55,989,914 , ATG14, 3 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
    nsv5562460sequence alteration1nstd206human GRCh38 chr14: 55,370,728-55,523,213 , GRCh37.p13 chr14: 55,837,446-55,989,931 , ATG14, 3 more genes
    nsv5555347sequence alteration1nstd206human GRCh38 chr14: 54,915,499-55,646,544 , GRCh37.p13 chr14: 55,382,217-56,113,262 , ATG14, 21 more genes
    nsv5504354copy number variation1nstd206human GRCh38 chr14: 55,374,365-55,374,567 , GRCh37.p13 chr14: 55,841,083-55,841,285 ATG14
    nsv5188616mobile element insertion1nstd203human GRCh38 chr14: 55,401,518-55,401,531 , GRCh37.p13 chr14: 55,868,236-55,868,249 ATG14
    nsv5147924mobile element insertion1nstd203human GRCh38 chr14: 55,394,683-55,394,697 , GRCh37.p13 chr14: 55,861,401-55,861,415 ATG14, HMGN1P1
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4999421copy number variation1nstd200human GRCh38 chr14: 55,374,630-55,376,435 , GRCh37.p13 chr14: 55,841,348-55,843,153 ATG14
    nsv4675883copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,615,073-58,043,694 , GRCh38.p12 chr14: 55,148,355-57,576,976 FBXO34-AS1, FBXO34, 39 more genes
    nsv4621400copy number variation1nstd183human GRCh37 chr14: 55,844,612-55,844,863 , GRCh38.p12 chr14: 55,377,894-55,378,145 ATG14
    nsv4620986copy number variation1nstd183human GRCh37 chr14: 55,812,782-55,908,436 , GRCh38.p12 chr14: 55,346,064-55,441,718 , ATG14, 4 more genes
    nsv4505006mobile element insertion1nstd166human GRCh37.p13 chr14: 55,855,501-55,855,501 , GRCh38.p12 chr14: 55,388,783-55,388,783 ATG14
    nsv4500104mobile element insertion1nstd166human GRCh37.p13 chr14: 55,864,566-55,864,566 , GRCh38.p12 chr14: 55,397,848-55,397,848 ATG14
    nsv4219204copy number variation1nstd166human GRCh37.p13 chr14: 55,869,607-55,869,675 , GRCh38.p12 chr14: 55,402,889-55,402,957 ATG14
    nsv4216429copy number variation1nstd166human GRCh37.p13 chr14: 55,848,065-55,920,476 , GRCh38.p12 chr14: 55,381,347-55,453,758 , ATG14, 3 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3916278copy number variation1nstd102humanPathogenic GRCh38 chr14: 50,591,011-56,286,919 , GRCh37 chr14: 51,057,729-56,753,637 , NCBI36 chr14: 50,127,479-55,823,390 LOC105370507, ATG14, 98 more genes
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