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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932769copy number variation1nstd209human GRCh38 chr17: 29,056,843-29,058,110 , GRCh37.p13 chr17: 27,383,861-27,385,128 PIPOX
    nsv5881530copy number variation1nstd209human GRCh38 chr17: 29,056,908-29,058,107 , GRCh37.p13 chr17: 27,383,926-27,385,125 PIPOX
    nsv5520740copy number variation1nstd206human GRCh38 chr17: 29,056,852-29,058,111 , GRCh37.p13 chr17: 27,383,870-27,385,129 PIPOX
    nsv5296558copy number variation1nstd204human GRCh38.p13 chr17: 29,056,608-29,058,107 , GRCh37.p13 chr17: 27,383,626-27,385,125 PIPOX
    nsv5280509copy number variation1nstd204human GRCh38.p13 chr17: 29,056,801-29,058,100 , GRCh37.p13 chr17: 27,383,819-27,385,118 PIPOX
    nsv5023919copy number variation1nstd200human GRCh38 chr17: 29,027,004-29,062,821 , GRCh37.p13 chr17: 27,354,022-27,389,839 PIPOX
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675321copy number variation1nstd102humanPathogenic GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689 ABHD15, LOC100420408, 112 more genes
    nsv4624535copy number variation1nstd183human GRCh37 chr17: 27,384,182-27,384,648 , GRCh38.p12 chr17: 29,057,164-29,057,630 PIPOX
    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
    nsv4379025copy number variation1nstd173human GRCh37 chr17: 25,307,567-27,710,963 , GRCh38.p12 chr17: 26,980,541-29,383,945 , MIR451A, 91 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
    nsv4242993copy number variation1nstd166human GRCh37.p13 chr17: 27,383,870-27,385,129 , GRCh38.p12 chr17: 29,056,852-29,058,111 PIPOX
    nsv3972367copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 25,403,446-31,685,464 , GRCh38.p12 chr17: 27,076,420-33,358,446 ASIC2, AK4P1, 190 more genes
    nsv3919950copy number variation1nstd102humanPathogenic NCBI36 chr17: 24,298,969-27,841,151 , GRCh37 chr17: 27,274,843-30,817,038 , GRCh38 chr17: 28,947,825-32,490,020 MIR365B, EFCAB5, 105 more genes
    nsv3917332copy number variation1nstd102humanUncertain significance GRCh37 chr17: 27,084,301-27,543,437 , GRCh38 chr17: 28,757,283-29,216,419 , NCBI36 chr17: 24,108,428-24,567,563 RPL31P58, LOC100421028, 16 more genes
    nsv3916884copy number variation1nstd102humanUncertain significance NCBI36 chr17: 24,137,711-25,589,217 , GRCh37.p13 chr17: 27,113,585-28,565,091 , GRCh38.p12 chr17: 28,786,567-30,238,073 MIR451B, SEZ6, 43 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
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
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