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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148108copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,095,256-15,492,591 , GRCh38.p12 chr17: 14,191,939-15,589,277 LOC105371545, TVP23C, 25 more genes
    nsv7148090copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,095,256-15,477,547 , GRCh38.p12 chr17: 14,191,939-15,574,233 TEKT3, CDRT15, 25 more genes
    nsv7098896copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,095,306-15,472,344 , GRCh38.p12 chr17: 14,191,989-15,569,030 CDRT4, LOC105371547, 25 more genes
    nsv7098894copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,095,306-15,466,762 , GRCh38.p12 chr17: 14,191,989-15,563,448 CDRT8, TVP23C, 24 more genes
    nsv7093401copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,110,127-15,472,344 , GRCh38.p12 chr17: 14,206,810-15,569,030 HS3ST3B1, PMP22, 25 more genes
    nsv6997359copy number variation1nstd229human GRCh38 chr17: 14,524,308-15,152,912 , GRCh37.p13 chr17: 14,427,625-15,056,229 CDRT8, LOC105371545, 7 more genes
    nsv6997307copy number variation1nstd229human GRCh38 chr17: 14,987,397-15,034,129 , GRCh37.p13 chr17: 14,890,714-14,937,446 CDRT7
    nsv6989858copy number variation1nstd229human GRCh38 chr17: 14,635,906-15,104,802 , GRCh37.p13 chr17: 14,539,223-15,008,119 CDRT8, LINC02096, 5 more genes
    nsv6989281copy number variation1nstd229human GRCh38 chr17: 15,016,871-15,035,490 , GRCh37.p13 chr17: 14,920,188-14,938,807 CDRT7
    nsv6986095copy number variation1nstd229human GRCh38 chr17: 14,701,506-15,057,043 , GRCh37.p13 chr17: 14,604,823-14,960,360 RPS18P12, LINC02096, 4 more genes
    nsv6979351copy number variation1nstd229human GRCh38 chr17: 12,688,917-15,327,390 , GRCh37.p13 chr17: 12,592,234-15,230,707 PMP22, COX10-DT, 32 more genes
    nsv6638035copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,087,934-15,484,630 , GRCh38.p12 chr17: 14,184,617-15,581,316 COX10, CDRT15, 25 more genes
    nsv6637965copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,083,055-15,484,859 , GRCh38.p12 chr17: 14,179,738-15,581,545 CDRT8, LOC105371545, 25 more genes
    nsv6637912copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,073,563-15,479,923 , GRCh38.p12 chr17: 14,170,246-15,576,609 TVP23C-CDRT4, LOC101928475, 25 more genes
    nsv6637838copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,082,945-15,484,858 , GRCh38.p12 chr17: 14,179,628-15,581,544 COX10, FBXW10B, 25 more genes
    nsv6637794copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,078,283-15,479,940 , GRCh38.p12 chr17: 14,174,966-15,576,626 LOC105371545, TVP23C, 25 more genes
    nsv6637650copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,083,055-15,483,608 , GRCh38.p12 chr17: 14,179,738-15,580,294 MGC12916, RPL9P2, 25 more genes
    nsv6637617copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,087,934-15,491,532 , GRCh38.p12 chr17: 14,184,617-15,588,218 MGC12916, RPL9P2, 25 more genes
    nsv6637613copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,087,788-15,484,858 , GRCh38.p12 chr17: 14,184,471-15,581,544 TVP23C-CDRT4, LOC105371547, 25 more genes
    nsv6637590copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,087,934-15,479,940 , GRCh38.p12 chr17: 14,184,617-15,576,626 LOC105371545, RN7SL792P, 25 more genes
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