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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148126copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,851,693-22,089,506 , GRCh38.p12 chr14: 21,383,534-21,621,353 OR10G3, SNORD9, 17 more genes
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv6957519copy number variation1nstd229human GRCh38 chr14: 21,558,101-21,568,100 , GRCh37.p13 chr14: 22,026,232-22,036,231 RBBP4P5, OR10G3
    nsv6941553copy number variation1nstd229human GRCh38 chr14: 21,556,701-21,568,200 , GRCh37.p13 chr14: 22,024,832-22,036,331 OR10G3, RBBP4P5
    nsv6940546copy number variation1nstd229human GRCh38 chr14: 21,568,901-21,571,700 , GRCh37.p13 chr14: 22,037,032-22,039,832 OR10G3
    nsv6939691copy number variation1nstd229human GRCh38 chr14: 21,566,797-21,569,937 , GRCh37.p13 chr14: 22,034,928-22,038,068 OR10G3, RBBP4P5
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 more genes
    nsv6495085copy number variation1nstd223human GRCh38 chr14: 21,554,739-21,568,814 , GRCh37.p13 chr14: 22,022,870-22,036,945 OR10G3, RBBP4P5
    nsv6489186copy number variation1nstd223human GRCh38 chr14: 21,565,801-21,569,200 , GRCh37.p13 chr14: 22,033,932-22,037,331 RBBP4P5, OR10G3
    nsv6486406copy number variation1nstd223human GRCh38 chr14: 21,538,051-22,772,225 , GRCh37.p13 chr14: 22,006,185-23,241,434 TRAJ54, TRAV9-1, 152 more genes
    nsv6484958copy number variation1nstd223human GRCh38 chr14: 21,560,101-21,568,100 , GRCh37.p13 chr14: 22,028,232-22,036,231 RBBP4P5, OR10G3
    nsv6479949copy number variation1nstd223human GRCh38 chr14: 21,563,501-21,568,800 , GRCh37.p13 chr14: 22,031,632-22,036,931 OR10G3, RBBP4P5
    nsv6478706copy number variation1nstd223human GRCh38 chr14: 21,564,301-21,568,400 , GRCh37.p13 chr14: 22,032,432-22,036,531 RBBP4P5, OR10G3
    nsv6476482copy number variation1nstd223human GRCh38 chr14: 21,559,201-21,568,100 , GRCh37.p13 chr14: 22,027,332-22,036,231 RBBP4P5, OR10G3
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6290276copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 20,925,965-23,649,548 , GRCh38.p12 chr14: 20,457,806-23,180,339 ANG, APEX1, 255 more genes
    nsv6132583copy number variation1nstd213human GRCh37 chr14: 20,420,000-22,590,001 , GRCh38.p12 chr14: 19,951,841-22,122,043 HNRNPC, PNP, 157 more genes
    nsv6121071copy number variation1nstd186human GRCh37 chr14: 22,026,284-22,036,288 , GRCh38.p12 chr14: 21,558,153-21,568,157 OR10G3, RBBP4P5
    nsv6026618copy number variation1nstd212human GRCh38 chr14: 21,567,372-21,568,754 , GRCh37.p13 chr14: 22,035,503-22,036,885 OR10G3
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