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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7095341copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,289,526-6,616,652 , GRCh38.p12 chr17: 5,386,206-6,713,333 RNA5SP435, DHX33, 31 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv6982450copy number variation1nstd229human GRCh38 chr17: 1,838,614-7,660,509 , GRCh37.p13 chr17: 1,741,908-7,563,827 NCBP3, OR1P1, 242 more genes
    nsv6637885copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,399,850-5,601,196 , GRCh38.p12 chr17: 5,496,530-5,697,876 LOC728392, LOC105371507, 3 more genes
    nsv6624289copy number variation1nstd224human GRCh37 chr17: 4,948,344-6,354,965 , GRCh38.p12 chr17: 5,045,049-6,451,645 C1QBP, NUP88, 32 more genes
    nsv6592364inversion1nstd223human GRCh38 chr17: 2,078,667-6,081,513 , GRCh37.p13 chr17: 1,981,961-5,984,833 MYBBP1A, CXCL16, 143 more genes
    nsv6589878inversion1nstd223human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 ASGR1, KIF1C-AS1, 321 more genes
    nsv6502891copy number variation1nstd223human GRCh38 chr17: 5,500,601-5,501,100 , GRCh37.p13 chr17: 5,403,921-5,404,420 NLRP1, LOC728392
    nsv6133245copy number variation1nstd213human GRCh37 chr17: 4,010,000-8,220,001 , GRCh38.p12 chr17: 4,106,706-8,316,683 ACADVL, ALOX12, 220 more genes
    nsv6133065copy number variation1nstd213human GRCh37 chr17: 4,530,000-8,270,001 , GRCh38.p12 chr17: 4,626,705-8,366,683 ACADVL, ALOX12, 206 more genes
    nsv6133064copy number variation1nstd213human GRCh37 chr17: 4,520,000-8,470,001 , GRCh38.p12 chr17: 4,616,705-8,566,683 ACADVL, ALOX12, 217 more genes
    nsv5031337inversion1nstd200human GRCh38 chr17: 5,462,212-6,246,469 , GRCh37.p13 chr17: 5,365,532-6,149,789 NLRP1, DHX33-DT, 12 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729877copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,143,295-5,850,209 , GRCh38.p12 chr17: 5,240,000-5,946,889 DHX33, MIS12, 14 more genes
    nsv4675776copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,378,522-5,692,834 , GRCh38.p12 chr17: 5,475,202-5,789,514 RNU7-31P, MIS12, 7 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4630208copy number variation1nstd183human GRCh37 chr17: 4,486,568-5,620,052 , GRCh38.p12 chr17: 4,583,273-5,716,732 , ARRB2, 59 more genes
    nsv4457587copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,759,126-6,128,911 , GRCh38.p12 chr17: 3,855,832-6,225,591 DERL2, ZZEF1, 82 more genes
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