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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148245copy number variation1nstd102humanPathogenic GRCh38 chr17: 29,461,486-29,495,582 , GRCh37.p13 chr17: 27,788,504-27,822,600 TAOK1
    nsv7148088copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,263,507-27,829,791 , GRCh38.p12 chr17: 26,936,481-29,502,773 RNU4-34P, RNU6-711P, 95 more genes
    nsv7137122copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 27,834,915-27,870,040 , GRCh38.p12 chr17: 29,507,897-29,543,022 TAOK1
    nsv7095086copy number variation1nstd102humanPathogenic GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139 LOC107984990, ADAP2, 59 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7064107inversion1nstd229human GRCh38 chr17: 29,541,522-29,542,149 , GRCh37.p13 chr17: 27,868,540-27,869,167 TAOK1
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv7061729inversion1nstd229human GRCh38 chr17: 29,525,077-29,526,162 , GRCh37.p13 chr17: 27,852,095-27,853,180 TAOK1
    nsv6996698copy number variation1nstd229human GRCh38 chr17: 29,462,601-29,542,600 , GRCh37.p13 chr17: 27,789,619-27,869,618 TAOK1
    nsv6992400copy number variation1nstd229human GRCh38 chr17: 29,481,542-29,481,677 , GRCh37.p13 chr17: 27,808,560-27,808,695 TAOK1
    nsv6991752copy number variation1nstd229human GRCh38 chr17: 29,439,175-29,439,268 , GRCh37.p13 chr17: 27,766,193-27,766,286 TAOK1
    nsv6991434copy number variation1nstd229human GRCh38 chr17: 29,432,762-29,438,020 , GRCh37.p13 chr17: 27,759,780-27,765,038 TAOK1
    nsv6991383copy number variation1nstd229human GRCh38 chr17: 29,422,047-29,423,259 , GRCh37.p13 chr17: 27,749,065-27,750,277 RNU6-711P, TAOK1
    nsv6991323copy number variation1nstd229human GRCh38 chr17: 29,414,009-29,418,490 , GRCh37.p13 chr17: 27,741,027-27,745,508 TAOK1
    nsv6990252copy number variation1nstd229human GRCh38 chr17: 29,421,933-29,423,244 , GRCh37.p13 chr17: 27,748,951-27,750,262 TAOK1, RNU6-711P
    nsv6989414copy number variation1nstd229human GRCh38 chr17: 29,485,512-29,488,401 , GRCh37.p13 chr17: 27,812,530-27,815,419 TAOK1
    nsv6984294copy number variation1nstd229human GRCh38 chr17: 29,394,280-29,420,207 , GRCh37.p13 chr17: 27,721,298-27,747,225 TAOK1
    nsv6982447copy number variation1nstd229human GRCh38 chr17: 29,457,019-29,465,069 , GRCh37.p13 chr17: 27,784,037-27,792,087 TAOK1
    nsv6982092copy number variation1nstd229human GRCh38 chr17: 29,407,917-29,412,074 , GRCh37.p13 chr17: 27,734,935-27,739,092 TAOK1
    nsv6981299copy number variation1nstd229human GRCh38 chr17: 29,455,171-29,457,308 , GRCh37.p13 chr17: 27,782,189-27,784,326 TAOK1
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