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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137103copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,664,739-20,370,783 , GRCh38.p12 chr17: 16,761,425-20,467,470 NMTRQ-TTG12-1, NOS2P4, 148 more genes
    nsv7098881copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,116,969-20,217,378 , GRCh38.p12 chr17: 17,213,655-20,314,065 LOC105371578, SNORD3B-2, 119 more genes
    nsv7093160copy number variation1nstd102humanPathogenic GRCh38 chr17: 18,856,298-20,402,192 , GRCh37.p13 chr17: 18,759,611-20,305,505 LOC100131943, GRAP, 53 more genes
    nsv7077458inversion1nstd229human GRCh38 chr17: 19,655,327-19,749,869 , GRCh37.p13 chr17: 19,558,640-19,653,182 SLC47A2, ALDH3A2, 1 more genes
    nsv7070653inversion1nstd229human GRCh38 chr17: 18,758,972-20,738,114 , GRCh37.p13 chr17: 18,662,285-20,641,427 LOC401875, LGALS9B, 81 more genes
    nsv7067217inversion1nstd229human GRCh38 chr17: 19,708,681-19,802,154 , GRCh37.p13 chr17: 19,611,994-19,705,467 ALDH3A1, ULK2, 2 more genes
    nsv7061998inversion1nstd229human GRCh38 chr17: 18,691,607-20,798,512 , GRCh37.p13 chr17: 18,594,920-20,701,825 RNU6-467P, SLC47A1P1, 86 more genes
    nsv7060840inversion1nstd229human GRCh38 chr17: 19,684,238-19,684,379 , GRCh37.p13 chr17: 19,587,551-19,587,692 SLC47A2
    nsv6997683copy number variation1nstd229human GRCh38 chr17: 19,662,495-19,905,171 , GRCh37.p13 chr17: 19,565,808-19,808,484 ULK2, NDUFB4P3, 6 more genes
    nsv6995249copy number variation1nstd229human GRCh38 chr17: 19,708,301-19,711,100 , GRCh37.p13 chr17: 19,611,614-19,614,413 SLC47A2
    nsv6992434copy number variation1nstd229human GRCh38 chr17: 19,704,352-19,719,901 , GRCh37.p13 chr17: 19,607,665-19,623,214 SLC47A2
    nsv6991921copy number variation1nstd229human GRCh38 chr17: 19,679,676-19,714,833 , GRCh37.p13 chr17: 19,582,989-19,618,146 SLC47A2
    nsv6991486copy number variation1nstd229human GRCh38 chr17: 19,685,207-19,694,299 , GRCh37.p13 chr17: 19,588,520-19,597,612 SLC47A2
    nsv6991302copy number variation1nstd229human GRCh38 chr17: 19,519,452-19,681,956 , GRCh37.p13 chr17: 19,422,765-19,585,269 SLC47A1, NMTRQ-TTG12-1, 8 more genes
    nsv6990481copy number variation1nstd229human GRCh38 chr17: 19,712,700-19,721,106 , GRCh37.p13 chr17: 19,616,013-19,624,419 SLC47A2
    nsv6986723copy number variation1nstd229human GRCh38 chr17: 19,714,204-19,716,487 , GRCh37.p13 chr17: 19,617,517-19,619,800 SLC47A2
    nsv6981567copy number variation1nstd229human GRCh38 chr17: 19,655,301-19,708,700 , GRCh37.p13 chr17: 19,558,614-19,612,013 ALDH3A2, SLC47A2
    nsv6980238copy number variation1nstd229human GRCh38 chr17: 19,707,170-19,713,339 , GRCh37.p13 chr17: 19,610,483-19,616,652 SLC47A2
    nsv6978400copy number variation1nstd229human GRCh38 chr17: 19,680,012-19,685,453 , GRCh37.p13 chr17: 19,583,325-19,588,766 SLC47A2
    nsv6637475copy number variation1nstd102humanUncertain significance GRCh37 chr17: 19,423,469-19,588,176 , GRCh38.p12 chr17: 19,520,156-19,684,863 MTND2P12, SNORA59B, 8 more genes
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