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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141307insertion1nstd232human GRCh37.p13 chr14: 20,823,100-20,823,100 , GRCh38.p12 chr14: 20,354,941-20,354,941 PARP2
    nsv6957164copy number variation1nstd229human GRCh38 chr14: 20,348,840-20,349,517 , GRCh37.p13 chr14: 20,816,999-20,817,676 PARP2
    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
    nsv6952855copy number variation1nstd229human GRCh38 chr14: 20,348,830-20,349,545 , GRCh37.p13 chr14: 20,816,989-20,817,704 PARP2
    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
    nsv6950783copy number variation1nstd229human GRCh38 chr14: 20,352,730-20,361,891 , GRCh37.p13 chr14: 20,820,889-20,830,050 PARP2
    nsv6946487copy number variation1nstd229human GRCh38 chr14: 20,349,997-20,357,286 , GRCh37.p13 chr14: 20,818,156-20,825,445 PARP2
    nsv6938400copy number variation1nstd229human GRCh38 chr14: 20,328,054-20,342,069 , GRCh37.p13 chr14: 20,796,213-20,810,228 CCNB1IP1, RPPH1, 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
    nsv6585331inversion1nstd223human GRCh38 chr14: 20,347,685-20,349,068 , GRCh37.p13 chr14: 20,815,844-20,817,227 PARP2
    nsv6492867copy number variation1nstd223human GRCh38 chr14: 20,335,061-20,343,011 , GRCh37.p13 chr14: 20,803,220-20,811,170 PARP2, RPPH1
    nsv6491048copy number variation1nstd223human GRCh38 chr14: 20,348,929-20,349,584 , GRCh37.p13 chr14: 20,817,088-20,817,743 PARP2
    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
    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
    nsv6249658mobile element insertion1nstd215human GRCh38 chr14: 20,343,057-20,343,057 , GRCh37.p13 chr14: 20,811,216-20,811,216 PARP2, RPPH1
    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
    nsv6040402copy number variation1nstd212human GRCh38 chr14: 20,347,360-20,347,421 , GRCh37.p13 chr14: 20,815,519-20,815,580 PARP2
    nsv5710683mobile element insertion1nstd211human GRCh38 chr14: 20,343,065-20,343,065 , GRCh37.p13 chr14: 20,811,224-20,811,224 RPPH1, PARP2
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