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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5729324mobile element insertion1nstd211human GRCh38 chr17: 81,848,573-81,848,573 , GRCh37.p13 chr17: 79,806,449-79,806,449 P4HB
    nsv5719653mobile element insertion1nstd211human GRCh38 chr17: 81,848,588-81,848,588 , GRCh37.p13 chr17: 79,806,464-79,806,464 P4HB
    nsv5528091copy number variation1nstd206human GRCh38 chr17: 81,849,376-81,853,454 , GRCh37.p13 chr17: 79,807,252-79,811,330 P4HB
    nsv5320535translocation1nstd204human GRCh38.p13 chr17: 81,841,126-81,841,126 , GRCh38.p13 chr17: 81,841,560-81,841,560 , GRCh37.p13 chr17: 79,799,002-79,799,002 , GRCh37.p13 chr17: 79,799,436-79,799,436 P4HB
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
    nsv5293265copy number variation1nstd204human GRCh38.p13 chr17: 81,856,901-81,865,700 , GRCh37.p13 chr17: 79,814,777-79,823,576 P4HB
    nsv5290477copy number variation1nstd204human GRCh38.p13 chr17: 81,742,501-82,145,800 , GRCh37.p13 chr17: 79,759,050-80,103,676 PPP1R27, MAFG, 27 more genes
    nsv5288922copy number variation1nstd204human GRCh37.p13 chr17: 79,777,077-79,870,376 , GRCh38.p13 chr17: 81,819,201-81,912,500 ARHGDIA, P4HB, 7 more genes
    nsv5017069copy number variation1nstd200human GRCh38 chr17: 81,859,319-81,862,866 , GRCh37.p13 chr17: 79,817,195-79,820,742 P4HB
    nsv4867540copy number variation1nstd200human GRCh37 chr17: 79,799,002-79,799,436 , GRCh38.p12 chr17: 81,841,126-81,841,560 P4HB
    nsv4671480copy number variation1nstd186human GRCh37 chr17: 79,807,255-79,811,342 , GRCh38.p12 chr17: 81,849,379-81,853,466 P4HB
    nsv4621301copy number variation1nstd183human GRCh37 chr17: 79,807,255-79,811,342 , GRCh38.p12 chr17: 81,849,379-81,853,466 P4HB
    nsv4619638copy number variation1nstd183human GRCh37 chr17: 79,785,999-81,060,000 , GRCh38.p12 chr17: 81,828,123-83,101,964 , PCYT2, 55 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4457495copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,663,313-80,197,463 , GRCh38.p12 chr17: 81,696,283-82,239,587 NOTUM, PPP1R27, 34 more genes
    nsv4457483copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,608,912-81,041,938 , GRCh38.p12 chr17: 80,635,112-83,084,062 HEXD, LOC105371929, 94 more genes
    nsv4374349copy number variation1nstd173human GRCh37 chr17: 79,330,617-80,189,678 , GRCh38.p12 chr17: 81,356,817-82,231,802 , FAAP100, 49 more genes
    nsv4271279copy number variation1nstd166human GRCh37.p13 chr17: 79,813,000-79,820,000 , GRCh38.p12 chr17: 81,855,124-81,862,124 P4HB
    nsv3919635copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677 LINC03048, MIR3186, 154 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
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