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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6994943copy number variation1nstd229human GRCh38 chr17: 56,890,787-56,890,974 , GRCh37.p13 chr17: 54,968,148-54,968,335 TRIM25, MIR3614
    nsv6981518copy number variation1nstd229human GRCh38 chr17: 56,905,795-56,909,113 , GRCh37.p13 chr17: 54,983,156-54,986,474 TRIM25
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv5976111insertion1nstd209human GRCh38 chr17: 56,893,223-56,893,223 , GRCh37.p13 chr17: 54,970,584-54,970,584 TRIM25
    nsv5932456copy number variation1nstd209human GRCh38 chr17: 56,895,613-56,902,151 , GRCh37.p13 chr17: 54,972,974-54,979,512 TRIM25
    nsv5873900copy number variation1nstd209human GRCh38 chr17: 56,895,770-56,902,069 , GRCh37.p13 chr17: 54,973,131-54,979,430 TRIM25
    nsv5659512insertion1nstd207human GRCh38 chr17: 56,893,223-56,893,223 , GRCh37.p13 chr17: 54,970,584-54,970,584 TRIM25
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5548560insertion1nstd206human GRCh38 chr17: 56,893,223-56,893,223 , GRCh37.p13 chr17: 54,970,584-54,970,584 TRIM25
    nsv5538633insertion1nstd206human GRCh38 chr17: 56,897,131-56,897,165 , GRCh37.p13 chr17: 54,974,492-54,974,526 TRIM25
    nsv5147815mobile element insertion1nstd203human GRCh38 chr17: 56,897,114-56,897,130 , GRCh37.p13 chr17: 54,974,475-54,974,491 TRIM25
    nsv4718592insertion1nstd186human GRCh37 chr17: 54,970,584-54,970,584 , GRCh38.p12 chr17: 56,893,223-56,893,223 TRIM25
    nsv4538626insertion1nstd166human GRCh37.p13 chr17: 54,974,475-54,974,475 , GRCh38.p12 chr17: 56,897,114-56,897,114 TRIM25
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4326333insertion1nstd166human GRCh37.p13 chr17: 54,970,584-54,970,584 , GRCh38.p12 chr17: 56,893,223-56,893,223 TRIM25
    nsv4259477copy number variation1nstd166human GRCh37.p13 chr17: 54,975,012-54,975,070 , GRCh38.p12 chr17: 56,897,651-56,897,709 TRIM25
    nsv3920623copy number variation1nstd102humanPathogenic GRCh37 chr17: 54,760,866-56,162,300 , NCBI36 chr17: 52,115,865-53,517,299 , GRCh38 chr17: 56,683,505-58,084,939 C17orf67, CUEDC1, 28 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
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