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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137094copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 44,949,883-46,507,482 , GRCh38.p12 chr17: 46,872,517-48,430,120 CDC27, ITGB3, 49 more genes
    nsv6992731copy number variation1nstd229human GRCh38 chr17: 47,116,036-47,169,410 , GRCh37.p13 chr17: 45,193,402-45,246,776 RPS2P47, LOC112268192, 1 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6978401copy number variation1nstd229human GRCh38 chr17: 47,159,523-47,163,891 , GRCh37.p13 chr17: 45,236,889-45,241,257 CDC27, RPS2P47
    nsv6624247copy number variation1nstd224human GRCh37 chr17: 45,194,762-45,249,360 , GRCh38.p12 chr17: 47,117,396-47,171,994 LOC112268192, CDC27, 1 more genes
    nsv6291459copy number variation1nstd102humanLikely benign GRCh37 chr17: 45,080,707-45,281,405 , GRCh38.p12 chr17: 47,003,341-47,204,039 RPS2P47, LOC101927060, 5 more genes
    nsv6133063copy number variation1nstd213human GRCh37 chr17: 45,180,000-45,790,001 , GRCh38.p12 chr17: 47,102,634-47,712,635 CDC27, NPEPPS, 14 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5541839insertion1nstd206human GRCh38 chr17: 47,157,452-47,157,452 , GRCh37.p13 chr17: 45,234,818-45,234,818 CDC27, RPS2P47
    nsv5013769copy number variation1nstd200human GRCh38 chr17: 47,116,036-47,169,410 , GRCh37.p13 chr17: 45,193,402-45,246,776 LOC112268192, CDC27, 1 more genes
    nsv4553287insertion1nstd166human GRCh37.p13 chr17: 45,234,818-45,234,818 , GRCh38.p12 chr17: 47,157,452-47,157,452 RPS2P47, CDC27
    nsv4436018complex substitution1nstd102humanUncertain significance GRCh37 chr17: 45,008,570-45,994,044 , GRCh38.p12 chr17: 46,931,204-47,916,678 CDC27, ITGB3, 30 more genes
    nsv4427685copy number variation1nstd174human GRCh37 chr17: 45,234,744-45,249,307 , GRCh38.p12 chr17: 47,157,378-47,171,941 CDC27, RPS2P47
    nsv4421020copy number variation1nstd174human GRCh37 chr17: 45,234,405-45,235,571 , GRCh38.p12 chr17: 47,157,039-47,158,205 RPS2P47, CDC27
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4268126copy number variation1nstd166human GRCh37.p13 chr17: 45,193,402-45,246,776 , GRCh38.p12 chr17: 47,116,036-47,169,410 CDC27, LOC112268192, 1 more genes
    nsv4255183copy number variation1nstd166human GRCh37.p13 chr17: 44,957,094-45,748,956 , GRCh38.p12 chr17: 46,879,728-47,671,590 MRPL45P2, KPNB1, 24 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
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