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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095371copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,618,104-79,894,690 , GRCh38.p12 chr17: 81,651,074-81,936,814 CCDC137, PPP1R27, 21 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6992077copy number variation1nstd229human GRCh38 chr17: 81,897,970-81,907,480 , GRCh37.p13 chr17: 79,855,846-79,865,356 NPB, ANAPC11, 1 more genes
    nsv6990561copy number variation1nstd229human GRCh38 chr17: 81,892,478-81,908,324 , GRCh37.p13 chr17: 79,850,354-79,866,200 ANAPC11, PCYT2, 1 more genes
    nsv6989096copy number variation1nstd229human GRCh38 chr17: 81,904,946-81,905,046 , GRCh37.p13 chr17: 79,862,822-79,862,922 PCYT2
    nsv6979513copy number variation1nstd229human GRCh38 chr17: 81,893,709-81,915,931 , GRCh37.p13 chr17: 79,851,585-79,873,807 SIRT7, ANAPC11, 2 more genes
    nsv6532529copy number variation1nstd223human GRCh38 chr17: 81,904,001-81,904,600 , GRCh37.p13 chr17: 79,861,877-79,862,476 PCYT2
    nsv6525507copy number variation1nstd223human GRCh38 chr17: 81,799,201-82,693,800 , GRCh37.p13 chr17: 79,759,050-80,651,676 CENPX, RFNG, 47 more genes
    nsv6521584copy number variation1nstd223human GRCh38 chr17: 81,899,721-81,900,000 , GRCh37.p13 chr17: 79,857,597-79,857,876 PCYT2, ANAPC11
    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
    nsv6307114copy number variation1nstd186human GRCh37 chr17: 79,819,009-79,857,009 , GRCh38.p12 chr17: 81,861,133-81,899,133 ARHGDIA, PCYT2, 2 more genes
    nsv6306796copy number variation1nstd186human GRCh37 chr17: 79,851,009-79,859,009 , GRCh38.p12 chr17: 81,893,133-81,901,133 PCYT2, ANAPC11, 1 more genes
    nsv6196818copy number variation1nstd214human GRCh38 chr17: 81,904,956-81,905,005 , GRCh37.p13 chr17: 79,862,832-79,862,881 PCYT2
    nsv6146104copy number variation1nstd206human GRCh38 chr17: 81,861,133-81,899,133 , GRCh37.p13 chr17: 79,819,009-79,857,009 ARHGDIA, PCYT2, 2 more genes
    nsv6145522copy number variation1nstd206human GRCh38 chr17: 81,904,948-81,905,046 , GRCh37.p13 chr17: 79,862,824-79,862,922 PCYT2
    nsv6144462copy number variation1nstd206human GRCh38 chr17: 81,893,133-81,901,133 , GRCh37.p13 chr17: 79,851,009-79,859,009 ANAPC11, NPB, 1 more genes
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
    nsv6024933copy number variation1nstd212human GRCh38 chr17: 81,904,962-81,905,013 , GRCh37.p13 chr17: 79,862,838-79,862,889 PCYT2
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