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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6957313copy number variation1nstd229human GRCh38 chr14: 20,322,976-20,336,434 , GRCh37.p13 chr14: 20,791,135-20,804,593 CCNB1IP1, SNORD126, 1 more genes
    nsv6956640copy number variation1nstd229human GRCh38 chr14: 20,319,368-20,350,049 , GRCh37.p13 chr14: 20,787,527-20,818,208 PARP2, RPPH1, 3 more genes
    nsv6950973copy number variation1nstd229human GRCh38 chr14: 20,013,858-20,436,718 , GRCh37.p13 chr14: 20,482,017-20,904,877 OR4L1, RNA5SP382, 25 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
    nsv6594921inversion1nstd223human GRCh38 chr14: 20,323,884-20,324,450 , GRCh37.p13 chr14: 20,792,043-20,792,609 CCNB1IP1, SNORD126
    nsv6494960copy number variation1nstd223human GRCh38 chr14: 20,323,701-20,325,400 , GRCh37.p13 chr14: 20,791,860-20,793,559 CCNB1IP1, SNORD126, 1 more genes
    nsv6487981copy number variation1nstd223human GRCh38 chr14: 20,013,858-20,436,718 , GRCh37.p13 chr14: 20,482,017-20,904,877 RNA5SP382, OR4L1, 25 more genes
    nsv6480239copy number variation1nstd223human GRCh38 chr14: 20,324,333-20,330,630 , GRCh37.p13 chr14: 20,792,492-20,798,789 SNORD126, CCNB1IP1
    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
    nsv6314064copy number variation1nstd102humanUncertain significance GRCh37 chr14: 20,664,697-21,017,250 , GRCh38.p12 chr14: 20,196,538-20,549,091 LOC100422510, SNORA79B, 20 more genes
    nsv6290645copy number variation1nstd102humanUncertain significance GRCh38 chr14: 20,013,858-20,436,718 , GRCh37.p13 chr14: 20,482,017-20,904,877 OR4T1P, OR11G1P, 25 more genes
    nsv6249657mobile element insertion1nstd215human GRCh38 chr14: 20,325,791-20,325,791 , GRCh37.p13 chr14: 20,793,950-20,793,950 CCNB1IP1, SNORD126
    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
    nsv6112958mobile element insertion1nstd186human GRCh37 chr14: 20,793,950-20,794,001 , GRCh38.p12 chr14: 20,325,791-20,325,842 SNORD126, CCNB1IP1
    nsv5976940insertion1nstd209human GRCh38 chr14: 20,325,775-20,325,775 , GRCh37.p13 chr14: 20,793,934-20,793,934 SNORD126, CCNB1IP1
    nsv5702193mobile element insertion2nstd211human GRCh38 chr14: 20,325,791-20,325,791 , GRCh37.p13 chr14: 20,793,950-20,793,950 SNORD126, CCNB1IP1
    nsv5657830insertion1nstd207human GRCh38 chr14: 20,325,775-20,325,775 , GRCh37.p13 chr14: 20,793,934-20,793,934 CCNB1IP1, SNORD126
    nsv5416275mobile element insertion1nstd206human GRCh38 chr14: 20,325,791-20,325,842 , GRCh37.p13 chr14: 20,793,950-20,794,001 SNORD126, CCNB1IP1
    nsv5157852mobile element insertion1nstd203human GRCh38 chr14: 20,325,775-20,325,791 , GRCh37.p13 chr14: 20,793,934-20,793,950 CCNB1IP1, SNORD126
    nsv5157734mobile element insertion1nstd203human GRCh38 chr14: 20,325,780-20,325,791 , GRCh37.p13 chr14: 20,793,939-20,793,950 SNORD126, CCNB1IP1
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