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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5498015copy number variation1nstd206human GRCh38 chr14: 34,191,713-38,057,713 , GRCh37.p13 chr14: 34,660,919-38,526,918 , RPL23AP71, 79 more genes
    nsv5381757copy number variation1nstd102humanPathogenic GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164 RPLP0P3, KRT18P6, 131 more genes
    nsv5261291copy number variation1nstd204human GRCh38.p13 chr14: 34,476,501-34,930,900 , GRCh37.p13 chr14: 34,945,707-35,400,106 CFL2, EAPP, 16 more genes
    nsv4994186copy number variation1nstd200human GRCh38 chr14: 34,504,452-34,707,225 , GRCh37.p13 chr14: 34,973,658-35,176,431 LOC105370449, LOC112268123, 10 more genes
    nsv4848075copy number variation1nstd200human GRCh37 chr14: 34,973,658-35,176,431 , GRCh38.p12 chr14: 34,504,452-34,707,225 RPS19P3, RPL23AP8, 10 more genes
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4683923copy number variation1nstd102humanUncertain significance GRCh37 chr14: 35,179,578-35,182,892 , GRCh38.p12 chr14: 34,710,372-34,713,686 CFL2
    nsv4680263copy number variation1nstd189human GRCh37.p13 chr14: 34,948,278-35,870,835 , GRCh38.p12 chr14: 34,479,072-35,401,629 CFL2, NFKBIA, 31 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4675386copy number variation1nstd102humanUncertain significance GRCh37 chr14: 34,939,747-35,257,173 , GRCh38.p12 chr14: 34,470,541-34,787,967 LOC112268123, LOC105370449, 13 more genes
    nsv4624427copy number variation1nstd183human GRCh37 chr14: 35,174,571-35,180,080 , GRCh38.p12 chr14: 34,705,365-34,710,874 CFL2
    nsv4455836copy number variation1nstd102humanUncertain significance GRCh37 chr14: 35,150,795-35,252,969 , GRCh38.p12 chr14: 34,681,589-34,783,763 RPL23AP8, LOC107984628, 3 more genes
    nsv4453660copy number variation1nstd102humanPathogenic GRCh38 chr14: 34,710,372-34,713,686 , GRCh37 chr14: 35,179,578-35,182,892 CFL2
    nsv3965757copy number variation1nstd168human GRCh38 chr14: 34,632,559-34,709,933 , GRCh37.p13 chr14: 35,101,765-35,179,139 CFL2, RPL23AP8, 2 more genes
    nsv3959314insertion1nstd168human GRCh38 chr14: 34,693,200-34,762,158 , GRCh37.p13 chr14: 35,162,406-35,231,364 CFL2, BAZ1A, 3 more genes
    nsv3924751copy number variation1nstd102humanPathogenic GRCh37 chr14: 31,261,477-45,154,334 , GRCh38 chr14: 30,792,271-44,685,131 , NCBI36 chr14: 30,331,228-44,224,084 DNAJC8P1, SNORA101B, 171 more genes
    nsv3922917copy number variation1nstd102humanPathogenic GRCh37 chr14: 30,851,760-38,181,546 , NCBI36 chr14: 29,921,511-37,251,297 , GRCh38 chr14: 30,382,554-37,712,341 MBIP, LOC105370447, 124 more genes
    nsv3921865copy number variation1nstd102humanUncertain significance NCBI36 chr14: 33,301,123-35,730,707 , GRCh37 chr14: 34,231,372-36,660,956 , GRCh38 chr14: 33,762,166-36,191,750 RPS19P3, LINC00609, 55 more genes
    nsv3920865copy number variation1nstd102humanUncertain significance GRCh38 chr14: 34,548,652-34,758,172 , GRCh37 chr14: 35,017,858-35,227,378 , NCBI36 chr14: 34,087,609-34,297,129 RNU6-1261P, RNU1-28P, 8 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
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