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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
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