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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv6957981copy number variation1nstd229human GRCh38 chr14: 21,797,883-22,503,752 , GRCh37.p13 chr14: 22,266,055-22,972,737 TRAV17, TRAV23DV6, 87 more genes
    nsv6956366copy number variation1nstd229human GRCh38 chr14: 21,769,088-22,542,200 , GRCh37.p13 chr14: 22,237,328-23,011,143 TRAV15, TRAJ61, 123 more genes
    nsv6955609copy number variation1nstd229human GRCh38 chr14: 21,749,702-22,503,765 , GRCh37.p13 chr14: 22,217,986-22,972,750 TRAV41, TRAJ58, 91 more genes
    nsv6946582copy number variation1nstd229human GRCh38 chr14: 21,749,701-22,503,751 , GRCh37.p13 chr14: 22,217,985-22,972,736 TRAJ40, TRAJ43, 91 more genes
    nsv6940530copy number variation1nstd229human GRCh38 chr14: 21,833,447-21,844,974 , GRCh37.p13 chr14: 22,301,604-22,313,156 TRAV12-1, TRA, 1 more genes
    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
    nsv6622464copy number variation1nstd224human GRCh37 chr14: 22,254,156-22,362,142 , GRCh38.p12 chr14: 21,785,940-21,893,962 TRAV8-4, TRAV8-1, 9 more genes
    nsv6490497copy number variation1nstd223human GRCh38 chr14: 21,805,301-21,896,800 , GRCh37.p13 chr14: 22,273,473-22,364,980 TRAV8-2, TRA, 8 more genes
    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
    nsv6479106copy number variation1nstd223human GRCh38 chr14: 21,765,668-21,857,377 , GRCh37.p13 chr14: 22,233,906-22,325,554 TRAV6, TRAV10, 8 more genes
    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
    nsv4994094copy number variation1nstd200human GRCh38 chr14: 21,778,204-21,852,216 , GRCh37.p13 chr14: 22,246,423-22,320,393 TRAV12-1, TRAV8-3, 7 more genes
    nsv4846760copy number variation1nstd200human GRCh37 chr14: 22,246,423-22,320,393 , GRCh38.p12 chr14: 21,778,204-21,852,216 TRA, TRAV10, 7 more genes
    nsv4728411copy number variation1nstd102humanUncertain significance GRCh37 chr14: 22,006,109-23,241,448 , GRCh38.p12 chr14: 21,537,975-22,772,239 OR4E2, TRAV10, 152 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
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
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