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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964563insertion1nstd209human GRCh38 chr8: 132,933,298-132,933,298 , GRCh37.p13 chr8: 133,945,543-133,945,543 TG
    nsv5963394insertion1nstd209human GRCh38 chr8: 132,908,422-132,908,422 , GRCh37.p13 chr8: 133,920,667-133,920,667 TG
    nsv5924959copy number variation1nstd209human GRCh38 chr8: 132,868,912-132,869,187 , GRCh37.p13 chr8: 133,881,157-133,881,432 TG
    nsv5918194copy number variation1nstd209human GRCh38 chr8: 133,022,840-133,023,562 , GRCh37.p13 chr8: 134,035,085-134,035,807 TG
    nsv5917534copy number variation1nstd209human GRCh38 chr8: 133,114,608-133,114,692 , GRCh37.p13 chr8: 134,126,852-134,126,936 TG
    nsv5908280copy number variation1nstd209human GRCh38 chr8: 133,033,312-133,033,365 , GRCh37.p13 chr8: 134,045,557-134,045,610 TG
    nsv5721156mobile element insertion1nstd211human GRCh38 chr8: 133,070,129-133,070,129 , GRCh37.p13 chr8: 134,082,374-134,082,374 SLA, TG
    nsv5715325mobile element insertion1nstd211human GRCh38 chr8: 132,945,089-132,945,089 , GRCh37.p13 chr8: 133,957,334-133,957,334 TG
    nsv5673945copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 133,141,509-134,296,554 , GRCh38.p12 chr8: 132,129,262-133,284,311 SLA, TMEM71, 15 more genes
    nsv5641649insertion1nstd207human GRCh38 chr8: 132,933,298-132,933,298 , GRCh37.p13 chr8: 133,945,543-133,945,543 TG
    nsv5639804insertion1nstd207human GRCh38 chr8: 132,908,422-132,908,422 , GRCh37.p13 chr8: 133,920,667-133,920,667 TG
    nsv5563361mobile element insertion1nstd206human GRCh38 chr8: 133,070,129-133,070,180 , GRCh37.p13 chr8: 134,082,374-134,082,425 SLA, TG
    nsv5549400insertion1nstd206human GRCh38 chr8: 132,908,422-132,908,422 , GRCh37.p13 chr8: 133,920,667-133,920,667 TG
    nsv5493735copy number variation1nstd206human GRCh38 chr8: 132,920,952-132,921,310 , GRCh37.p13 chr8: 133,933,197-133,933,555 TG
    nsv5492170copy number variation1nstd206human GRCh38 chr8: 133,022,840-133,023,571 , GRCh37.p13 chr8: 134,035,085-134,035,816 TG
    nsv5487770copy number variation1nstd206human GRCh38 chr8: 132,868,244-132,876,025 , GRCh37.p13 chr8: 133,880,489-133,888,270 TG
    nsv5478802copy number variation1nstd206human GRCh38 chr8: 132,925,362-132,930,094 , GRCh37.p13 chr8: 133,937,607-133,942,339 TG
    nsv5478439copy number variation1nstd206human GRCh38 chr8: 132,868,912-132,869,190 , GRCh37.p13 chr8: 133,881,157-133,881,435 TG
    nsv5364430translocation1nstd200human GRCh38 chr8: 132,915,550-132,915,550 , GRCh38 chr8: 132,915,628-132,915,628 , GRCh37.p13 chr8: 133,927,795-133,927,795 , GRCh37.p13 chr8: 133,927,873-133,927,873 TG
    nsv5343029translocation1nstd200human GRCh37 chr8: 134,126,853-134,126,853 , GRCh37 chr8: 134,126,937-134,126,937 , GRCh38.p12 chr8: 133,114,693-133,114,693 , GRCh38.p12 chr8: 133,114,609-133,114,609 TG
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