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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
    nsv7140437copy number variation1nstd232human GRCh37.p13 chr17: 3,584,003-3,584,072 , GRCh38.p12 chr17: 3,680,709-3,680,778 P2RX5, P2RX5-TAX1BP3
    nsv7095331copy number variation1nstd102humanPathogenic GRCh37 chr17: 3,379,454-3,819,519 , GRCh38.p12 chr17: 3,476,160-3,916,225 P2RX5-TAX1BP3, LOC100422717, 17 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
    nsv7068216inversion1nstd229human GRCh38 chr17: 3,683,142-3,696,091 , GRCh37.p13 chr17: 3,586,436-3,599,385 P2RX5, P2RX5-TAX1BP3
    nsv6995564copy number variation1nstd229human GRCh38 chr17: 3,396,087-3,729,964 , GRCh37.p13 chr17: 3,299,381-3,633,258 CTNS-AS1, ITGAE, 17 more genes
    nsv6987638copy number variation1nstd229human GRCh38 chr17: 3,669,235-3,673,212 , GRCh37.p13 chr17: 3,572,529-3,576,506 EMC6, P2RX5, 1 more genes
    nsv6982770copy number variation1nstd229human GRCh38 chr17: 3,468,201-5,384,400 , GRCh37.p13 chr17: 3,371,495-5,287,720 SLC25A11, CAMKK1, 83 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
    nsv6637211copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,392,984-3,631,198 , GRCh38.p12 chr17: 3,489,690-3,727,904 TRPV3, SPATA22, 14 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
    nsv6513205copy number variation1nstd223human GRCh38 chr17: 3,396,087-3,729,964 , GRCh37.p13 chr17: 3,299,381-3,633,258 LOC105371493, HASPIN, 17 more genes
    nsv6509238copy number variation1nstd223human GRCh38 chr17: 3,674,772-4,165,463 , GRCh37.p13 chr17: 3,578,066-4,068,757 P2RX5, ATP2A3, 11 more genes
    nsv6506401copy number variation1nstd223human GRCh38 chr17: 2,625,215-3,955,354 , GRCh37.p13 chr17: 2,528,509-3,858,648 CLUH, EMC6, 47 more genes
    nsv6496002copy number variation1nstd223human GRCh38 chr17: 3,564,725-4,578,738 , GRCh37.p13 chr17: 3,468,019-4,482,033 HASPIN, LOC100420060, 31 more genes
    nsv6310130copy number variation1nstd102humanPathogenic GRCh37 chr17: 2,541,583-3,819,519 , GRCh38.p12 chr17: 2,638,289-3,916,225 ASPA, EMC6, 46 more genes
    nsv6306160copy number variation1nstd186human GRCh37 chr17: 3,588,950-3,591,181 , GRCh38.p12 chr17: 3,685,656-3,687,887 P2RX5-TAX1BP3, P2RX5
    nsv6291554copy number variation1nstd102humanUncertain significance GRCh37 chr17: 2,646,815-3,698,838 , GRCh38.p12 chr17: 2,743,521-3,795,544 OR1D2, OR1A1, 37 more genes
    nsv6275457copy number variation1nstd214human GRCh38 chr17: 3,680,427-3,680,496 , GRCh37.p13 chr17: 3,583,721-3,583,790 P2RX5-TAX1BP3, P2RX5
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