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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv6996812copy number variation1nstd229human GRCh38 chr17: 75,830,143-75,898,563 , GRCh37.p13 chr17: 73,826,224-73,894,644 WBP2, UNC13D, 3 more genes
    nsv6996497copy number variation1nstd229human GRCh38 chr17: 75,879,296-75,883,357 , GRCh37.p13 chr17: 73,875,377-73,879,438 TRIM65
    nsv6992910copy number variation1nstd229human GRCh38 chr17: 75,883,689-75,922,201 , GRCh37.p13 chr17: 73,879,770-73,918,282 TRIM65, MRPL38, 1 more genes
    nsv6990286copy number variation1nstd229human GRCh38 chr17: 75,879,201-75,883,300 , GRCh37.p13 chr17: 73,875,282-73,879,381 TRIM65
    nsv6986823copy number variation1nstd229human GRCh38 chr17: 75,879,301-75,884,500 , GRCh37.p13 chr17: 73,875,382-73,880,581 TRIM65
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6983178copy number variation1nstd229human GRCh38 chr17: 75,896,306-75,896,427 , GRCh37.p13 chr17: 73,892,387-73,892,508 TRIM65
    nsv6980534copy number variation1nstd229human GRCh38 chr17: 75,879,302-75,883,323 , GRCh37.p13 chr17: 73,875,383-73,879,404 TRIM65
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6534054copy number variation1nstd223human GRCh38 chr17: 75,879,344-75,894,764 , GRCh37.p13 chr17: 73,875,425-73,890,845 TRIM65
    nsv6532077copy number variation1nstd223human GRCh38 chr17: 75,880,601-75,883,700 , GRCh37.p13 chr17: 73,876,682-73,879,781 TRIM65
    nsv6531768copy number variation1nstd223human GRCh38 chr17: 75,879,101-75,882,300 , GRCh37.p13 chr17: 73,875,182-73,878,381 TRIM65
    nsv6525343copy number variation1nstd223human GRCh38 chr17: 75,886,401-75,888,200 , GRCh37.p13 chr17: 73,882,482-73,884,281 TRIM65
    nsv6523948copy number variation1nstd223human GRCh38 chr17: 75,896,316-75,907,681 , GRCh37.p13 chr17: 73,892,397-73,903,762 TRIM65, MRPL38, 1 more genes
    nsv6519689copy number variation1nstd223human GRCh38 chr17: 75,883,686-75,922,197 , GRCh37.p13 chr17: 73,879,767-73,918,278 MRPL38, TRIM65, 1 more genes
    nsv6518961copy number variation1nstd223human GRCh38 chr17: 75,884,101-75,886,300 , GRCh37.p13 chr17: 73,880,182-73,882,381 TRIM65
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv5939145copy number variation1nstd209human GRCh38 chr17: 75,879,289-75,883,348 , GRCh37.p13 chr17: 73,875,370-73,879,429 TRIM65
    nsv5935589copy number variation1nstd209human GRCh38 chr17: 75,866,413-75,889,112 , GRCh37.p13 chr17: 73,862,494-73,885,193 TRIM65, TRIM47
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