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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5895203copy number variation1nstd209human GRCh38 chr3: 186,071,683-186,072,092 , GRCh37.p13 chr3: 185,789,472-185,789,881 ETV5
    nsv5572028copy number variation1nstd207human GRCh38 chr3: 186,071,683-186,072,092 , GRCh37.p13 chr3: 185,789,472-185,789,881 ETV5
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5450200copy number variation1nstd206human GRCh38 chr3: 186,087,071-186,088,361 , GRCh37.p13 chr3: 185,804,860-185,806,150 ETV5
    nsv5442148copy number variation1nstd206human GRCh38 chr3: 186,074,799-186,074,988 , GRCh37.p13 chr3: 185,792,588-185,792,777 ETV5
    nsv5387940copy number variation1nstd186human GRCh37 chr3: 185,789,506-185,789,882 , GRCh38.p12 chr3: 186,071,717-186,072,093 ETV5
    nsv5352297translocation1nstd200human GRCh38 chr3: 186,071,709-186,071,709 , GRCh38 chr3: 186,072,093-186,072,093 , GRCh37.p13 chr3: 185,789,882-185,789,882 , GRCh37.p13 chr3: 185,789,498-185,789,498 ETV5
    nsv5313060copy number variation1nstd204human GRCh38.p13 chr3: 186,071,571-186,072,310 , GRCh37.p13 chr3: 185,789,360-185,790,099 ETV5
    nsv5236290copy number variation1nstd204human GRCh38.p13 chr3: 186,060,481-186,070,671 , GRCh37.p13 chr3: 185,778,270-185,788,460 ETV5
    nsv5229066copy number variation1nstd204human GRCh37.p13 chr3: 185,406,289-185,899,189 , GRCh38.p13 chr3: 185,688,501-186,181,400 DGKG, ETV5, 6 more genes
    nsv5098644mobile element insertion1nstd203human GRCh38 chr3: 186,102,985-186,102,997 , GRCh37.p13 chr3: 185,820,774-185,820,786 ETV5
    nsv5087412mobile element insertion1nstd203human GRCh38 chr3: 186,092,734-186,092,748 , GRCh37.p13 chr3: 185,810,523-185,810,537 ETV5
    nsv4921277copy number variation1nstd200human GRCh38 chr3: 186,074,795-186,074,883 , GRCh37.p13 chr3: 185,792,584-185,792,672 ETV5
    nsv4798963copy number variation1nstd200human GRCh37 chr3: 185,789,410-185,789,956 , GRCh38.p12 chr3: 186,071,621-186,072,167 ETV5
    nsv4728604copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971 LOC105374253, GPS2P2, 111 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4674171copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 183,789,584-186,034,649 , GRCh38.p12 chr3: 184,071,796-186,316,860 AP2M1, CLCN2, 54 more genes
    nsv4648979copy number variation1nstd186human GRCh37 chr3: 185,789,307-185,789,882 , GRCh38.p12 chr3: 186,071,518-186,072,093 ETV5
    nsv4554072insertion1nstd166human GRCh37.p13 chr3: 185,820,774-185,820,774 , GRCh38.p12 chr3: 186,102,985-186,102,985 ETV5
    nsv4542814insertion1nstd166human GRCh37.p13 chr3: 185,820,726-185,820,726 , GRCh38.p12 chr3: 186,102,937-186,102,937 ETV5
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