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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6128748insertion1nstd186human GRCh37 chrX: 109,327,605-109,327,628 , GRCh38.p12 chrX: 110,084,377-110,084,400 TMEM164
    nsv6112702copy number variation1nstd102humanPathogenic GRCh37 chrX: 108,168,780-109,606,201 , GRCh38.p12 chrX: 108,925,550-110,362,973 MIR652, GNG5B, 14 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5978517copy number variation1nstd209human GRCh38 chrX: 110,072,342-110,080,182 , GRCh37.p13 chrX: 109,315,570-109,323,410 MIR3978, TMEM164
    nsv5976538copy number variation1nstd209human GRCh38 chrX: 110,176,618-110,195,125 , GRCh37.p13 chrX: 109,419,846-109,438,353 AMMECR1, TMEM164
    nsv5966938insertion1nstd209human GRCh38 chrX: 110,084,349-110,084,349 , GRCh37.p13 chrX: 109,327,577-109,327,577 TMEM164
    nsv5882109copy number variation1nstd209human GRCh38 chrX: 110,070,789-110,094,561 , GRCh37.p13 chrX: 109,314,017-109,337,789 MIR3978, TMEM164
    nsv5871464copy number variation1nstd209human GRCh38 chrX: 110,180,512-110,195,329 , GRCh37.p13 chrX: 109,423,740-109,438,557 TMEM164, AMMECR1
    nsv5731042mobile element insertion2nstd211human GRCh38 chrX: 110,043,824-110,043,824 , GRCh37.p13 chrX: 109,287,052-109,287,052 TMEM164
    nsv5727938mobile element insertion1nstd211human GRCh38 chrX: 110,169,680-110,169,680 , GRCh37.p13 chrX: 109,412,908-109,412,908 TMEM164
    nsv5723643mobile element insertion1nstd211human GRCh38 chrX: 110,108,068-110,108,068 , GRCh37.p13 chrX: 109,351,296-109,351,296 TMEM164
    nsv5671598copy number variation1nstd207human GRCh38 chrX: 110,048,092-110,048,149 , GRCh37.p13 chrX: 109,291,320-109,291,377 TMEM164
    nsv5623733insertion1nstd207human GRCh38 chrX: 110,084,349-110,084,349 , GRCh37.p13 chrX: 109,327,577-109,327,577 TMEM164
    nsv5547333insertion1nstd206human GRCh38 chrX: 110,084,377-110,084,400 , GRCh37.p13 chrX: 109,327,605-109,327,628 TMEM164
    nsv5431129copy number variation1nstd206human GRCh38 chrX: 110,070,988-110,072,055 , GRCh37.p13 chrX: 109,314,216-109,315,283 TMEM164
    nsv5427174copy number variation1nstd206human GRCh38 chrX: 110,072,941-110,075,449 , GRCh37.p13 chrX: 109,316,169-109,318,677 TMEM164
    nsv5426875copy number variation1nstd206human GRCh38 chrX: 110,099,050-110,100,879 , GRCh37.p13 chrX: 109,342,278-109,344,107 TMEM164
    nsv5425766copy number variation1nstd206human GRCh38 chrX: 110,147,454-110,147,741 , GRCh37.p13 chrX: 109,390,682-109,390,969 TMEM164
    nsv5416472copy number variation1nstd206human GRCh38 chrX: 110,070,789-110,094,562 , GRCh37.p13 chrX: 109,314,017-109,337,790 MIR3978, TMEM164
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