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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5872033copy number variation1nstd209human GRCh38 chr17: 39,023,377-39,030,780 , GRCh37.p13 chr17: 37,179,630-37,187,033 LRRC37A11P, LINC02079, 1 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5528475copy number variation1nstd206human GRCh38 chr17: 39,025,408-39,027,947 , GRCh37.p13 chr17: 37,181,661-37,184,200 LOC105371767, LINC02079, 1 more genes
    nsv5029089copy number variation1nstd200human GRCh38 chr17: 39,024,796-39,067,163 , GRCh37.p13 chr17: 37,181,049-37,223,416 LOC105371767, RDM1P5, 3 more genes
    nsv5029084copy number variation1nstd200human GRCh38 chr17: 38,907,869-39,140,425 , GRCh37.p13 chr17: 37,064,122-37,296,678 FBXO47, RDM1P5, 7 more genes
    nsv5016264copy number variation1nstd200human GRCh38 chr17: 39,027,012-39,027,073 , GRCh37.p13 chr17: 37,183,265-37,183,326 LINC02079, LOC105371767
    nsv4675332copy number variation1nstd102humanUncertain significance GRCh37 chr17: 36,710,984-37,295,662 , GRCh38.p12 chr17: 38,600,767-39,139,409 PIP4K2B, PSMB3, 32 more genes
    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
    nsv4262107copy number variation1nstd166human GRCh37.p13 chr17: 37,157,512-37,511,789 , GRCh38.p12 chr17: 39,001,259-39,355,536 LOC101929578, ARL5C, 13 more genes
    nsv4252691copy number variation1nstd166human GRCh37.p13 chr17: 37,183,265-37,183,326 , GRCh38.p12 chr17: 39,027,012-39,027,073 LOC105371767, LINC02079
    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
    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
    nsv3905679copy number variation1nstd102humanBenign GRCh37 chr17: 37,042,006-37,224,929 , GRCh38.p12 chr17: 38,885,753-39,068,676 PLXDC1, LRRC37A11P, 7 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3903293copy number variation1nstd102humanUncertain significance GRCh37 chr17: 36,972,794-38,033,708 , GRCh38.p12 chr17: 38,816,541-39,877,455 LASP1NB, MED1, 46 more genes
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