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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943104copy number variation1nstd209human GRCh38 chr17: 36,084,088-36,190,322 , GRCh37.p13 chr17|NW_003315949.1: 1-65,496 , TBC1D3B, 8 more genes
    nsv5941616copy number variation1nstd209human GRCh38 chr17: 36,083,984-36,190,304 , GRCh37.p13 chr17|NW_003315949.1: 1-65,496 , LOC101927369, 8 more genes
    nsv5873071copy number variation1nstd209human GRCh38 chr17: 36,082,782-36,093,326 , GRCh37.p13 chr17: 34,410,139-34,420,674 CCL3-AS1, CCL3
    nsv5870899copy number variation1nstd209human GRCh38 chr17: 36,085,581-36,093,054 , GRCh37.p13 chr17: 34,412,938-34,420,402 CCL3, CCL3-AS1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5323717copy number variation1nstd204human GRCh38.p13 chr17: 36,088,607-36,195,930 , GRCh37.p13 chr17|NW_003315949.1: 1-65,886 , LOC101927369, 9 more genes
    nsv5298268copy number variation1nstd204human GRCh38.p13 chr17: 36,083,937-36,092,529 , GRCh37.p13 chr17: 34,411,294-34,419,877 CCL3-AS1, CCL3
    nsv5294744copy number variation1nstd204human GRCh37.p13 chr17: 34,410,339-34,442,620 , GRCh38.p13 chr17: 36,082,982-36,121,014 CCL3, CCL4, 5 more genes
    nsv5281819copy number variation1nstd204human GRCh38.p13 chr17: 36,084,583-36,108,528 , GRCh37.p13 chr17: 34,411,940-34,435,921 LOC101927369, CCL3, 3 more genes
    nsv5280704copy number variation1nstd204human GRCh37.p13 chr17: 34,417,683-34,442,620 , GRCh38.p13 chr17: 36,090,337-36,120,226 CCL3, CCL4, 5 more genes
    nsv5029058copy number variation1nstd200human GRCh38 chr17: 36,087,385-36,194,121 , GRCh37.p13 chr17|NW_003315949.1: 1-65,530 , LOC107985055, 9 more genes
    nsv5029057copy number variation1nstd200human GRCh38 chr17: 36,080,948-36,147,850 , GRCh37.p13 chr17: 34,408,306-34,442,620 , CCL4, 6 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729906copy number variation1nstd102humanUncertain significance GRCh37 chr17: 34,405,241-34,823,294 , GRCh38.p12 chr17|NT_187614.1: 312,769-702,346 LOC100419980, LOC107985055, 19 more genes
    nsv4684339copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,360,168-36,209,228 , GRCh38 chr17|NT_187614.1: 267,696-2,088,293 , NCBI36 chr17: 31,384,281-33,283,341 TADA2A, SYNRG, 58 more genes
    nsv4684331copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,310,998-36,297,053 , GRCh38 chr17|NT_187614.1: 218,526-2,142,084 , NCBI36 chr17: 31,335,111-33,373,530 DUSP14, LOC105371757, 62 more genes
    nsv4684299copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,384,281-33,322,972 , GRCh38 chr17|NT_187614.1: 267,696-2,127,924 , GRCh37 chr17: 34,360,168-36,248,859 DHRS11, LOC100419980, 58 more genes
    nsv4675787copy number variation1nstd102humanUncertain significance GRCh37 chr17: 34,158,619-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 CCL4, CCL3-AS1, 15 more genes
    nsv4671929copy number variation2nstd186human GRCh37 chr17: 34,415,625-34,417,170 , GRCh38.p12 chr17: 36,088,279-36,089,824 , GRCh38.p12 chr17|NT_187661.1: 42,376-43,921 , GRCh38.p12 chr17|NT_187614.1: 323,153-324,698 CCL3-AS1, CCL3
    nsv4668486copy number variation2nstd186human GRCh37 chr17: 34,405,315-34,432,623 , GRCh38.p12 chr17: 36,077,955-36,105,230 , GRCh38.p12 chr17|NT_187661.1: 32,052-59,327 , GRCh38.p12 chr17|NT_187614.1: 312,843-340,151 CCL3, CCL4, 2 more genes
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