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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5646439insertion1nstd207human GRCh38 chr17: 40,490,409-40,490,409 , GRCh37.p13 chr17: 38,646,661-38,646,661 TNS4
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5532227copy number variation1nstd206human GRCh38 chr17: 40,483,094-40,504,893 , GRCh37.p13 chr17: 38,639,346-38,661,145 TNS4
    nsv5531885copy number variation1nstd206human GRCh38 chr17: 40,501,227-40,504,446 , GRCh37.p13 chr17: 38,657,479-38,660,698 TNS4
    nsv5016334copy number variation1nstd200human GRCh38 chr17: 40,492,906-40,494,525 , GRCh37.p13 chr17: 38,649,158-38,650,777 TNS4
    nsv5016333copy number variation1nstd200human GRCh38 chr17: 40,492,672-40,492,766 , GRCh37.p13 chr17: 38,648,924-38,649,018 TNS4
    nsv5016332copy number variation1nstd200human GRCh38 chr17: 40,479,425-40,481,563 , GRCh37.p13 chr17: 38,635,677-38,637,815 TNS4
    nsv5016330copy number variation1nstd200human GRCh38 chr17: 40,463,398-40,474,987 , GRCh37.p13 chr17: 38,619,650-38,631,239 , TNS4
    nsv4858793copy number variation1nstd200human GRCh37 chr17: 38,648,924-38,649,018 , GRCh38.p12 chr17: 40,492,672-40,492,766 TNS4
    nsv4623206copy number variation1nstd183human GRCh37 chr17: 38,588,234-38,671,817 , GRCh38.p12 chr17: 40,431,982-40,515,565 , TNS4, 3 more genes
    nsv4532344copy number variation1nstd166human GRCh37.p13 chr17: 38,648,874-38,649,018 , GRCh38.p12 chr17: 40,492,622-40,492,766 TNS4
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4266440copy number variation1nstd166human GRCh37.p13 chr17: 38,649,083-38,650,844 , GRCh38.p12 chr17: 40,492,831-40,494,592 TNS4
    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
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 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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