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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5303224copy number variation1nstd204human GRCh38.p13 chr14: 37,973,892-39,705,239 , GRCh37.p13 chr14: 38,443,097-40,174,443 RPL7AP2, LOC112268136, 25 more genes
    nsv5278802copy number variation1nstd204human GRCh38.p13 chr14: 38,101,201-39,697,400 , GRCh37.p13 chr14: 38,570,406-40,166,604 LOC100313942, PNN, 24 more genes
    nsv5266833copy number variation1nstd204human GRCh38.p13 chr14: 39,175,513-39,177,212 , GRCh37.p13 chr14: 39,644,717-39,646,416 PNN
    nsv4994225copy number variation1nstd200human GRCh38 chr14: 39,133,160-39,270,705 , GRCh37.p13 chr14: 39,602,364-39,739,909 PNN, RPL7AP2, 6 more genes
    nsv4994217copy number variation1nstd200human GRCh38 chr14: 37,973,902-39,705,237 , GRCh37.p13 chr14: 38,443,107-40,174,441 LOC100422334, TRAPPC6B, 25 more genes
    nsv4844239copy number variation1nstd200human GRCh37 chr14: 38,443,107-40,174,441 , GRCh38.p12 chr14: 37,973,902-39,705,237 LOC105370460, LOC102723516, 25 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
    nsv4676032copy number variation1nstd102humanPathogenic GRCh37 chr14: 36,830,396-42,541,277 , GRCh38.p12 chr14: 36,361,190-42,072,074 PPIAP4, LOC100533628, 60 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
    nsv4675897copy number variation1nstd102humanUncertain significance GRCh37 chr14: 39,444,420-39,903,666 , GRCh38.p12 chr14: 38,975,216-39,434,462 TRAPPC6B, GEMIN2, 13 more genes
    nsv4675716copy number variation1nstd102humanUncertain significance GRCh37 chr14: 39,570,335-39,854,035 , GRCh38.p12 chr14: 39,101,131-39,384,831 PPIAP4, MIA2, 11 more genes
    nsv4629131copy number variation1nstd183human GRCh37 chr14: 39,651,321-39,656,170 , GRCh38.p12 chr14: 39,182,117-39,186,966 PNN
    nsv4621139copy number variation1nstd183human GRCh37 chr14: 39,644,442-39,647,176 , GRCh38.p12 chr14: 39,175,238-39,177,972 PNN
    nsv4217138copy number variation1nstd166human GRCh37.p13 chr14: 39,652,903-39,653,716 , GRCh38.p12 chr14: 39,183,699-39,184,512 PNN
    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
    nsv3924371copy number variation1nstd102humanUncertain significance GRCh38 chr14: 38,828,029-40,664,503 , NCBI36 chr14: 38,366,984-40,203,458 , GRCh37 chr14: 39,297,233-41,133,708 GEMIN2, TRAPPC6B, 24 more genes
    nsv3921621copy number variation1nstd102humanPathogenic GRCh38 chr14: 36,434,568-41,102,476 , GRCh37 chr14: 36,903,773-41,571,681 , NCBI36 chr14: 35,973,524-40,641,431 CLEC14A, LOC105370456, 54 more genes
    nsv3921024copy number variation1nstd102humanPathogenic GRCh37 chr14: 35,537,482-44,463,980 , GRCh38 chr14: 35,068,276-43,994,777 , NCBI36 chr14: 34,607,233-43,533,730 LOC107984681, SLC25A21-AS1, 101 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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