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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932480copy number variation1nstd209human GRCh38 chr17: 737,101-786,197 , GRCh37.p13 chr17: 640,341-689,437 GEMIN4, GLOD4, 3 more genes
    nsv5880460copy number variation1nstd209human GRCh38 chr17: 737,735-747,334 , GRCh37.p13 chr17: 640,975-650,574 TLCD3A, GEMIN4
    nsv5876165copy number variation1nstd209human GRCh38 chr17: 742,235-743,634 , GRCh37.p13 chr17: 645,475-646,874 TLCD3A, GEMIN4
    nsv5660381insertion1nstd207human GRCh38 chr17: 753,305-753,305 , GRCh37.p13 chr17: 656,545-656,545 DBIL5P, GEMIN4
    nsv5651746insertion1nstd207human GRCh38 chr17: 749,003-749,003 , GRCh37.p13 chr17: 652,243-652,243 GEMIN4
    nsv5647302insertion1nstd207human GRCh38 chr17: 749,036-749,036 , GRCh37.p13 chr17: 652,276-652,276 GEMIN4
    nsv5596952copy number variation1nstd207human GRCh38 chr17: 753,052-753,142 , GRCh37.p13 chr17: 656,292-656,382 GEMIN4, DBIL5P
    nsv5558087sequence alteration1nstd206human GRCh38 chr17: 737,671-743,106 , GRCh37.p13 chr17: 640,911-646,346 GEMIN4, TLCD3A
    nsv5554903sequence alteration1nstd206human GRCh38 chr17: 662,533-1,370,380 , GRCh37.p13 chr17: 565,773-1,273,674 , YWHAE, 19 more genes
    nsv5527599copy number variation1nstd206human GRCh38 chr17: 737,635-743,155 , GRCh37.p13 chr17: 640,875-646,395 TLCD3A, GEMIN4
    nsv5523663copy number variation1nstd206human GRCh38 chr17: 425,022-895,616 , GRCh37.p13 chr17: 396,587-798,856 GEMIN4, GLOD4, 7 more genes
    nsv5390594copy number variation1nstd186human GRCh37 chr17: 651,942-652,278 , GRCh38.p12 chr17: 748,702-749,038 GEMIN4
    nsv5374762translocation1nstd200human GRCh38 chr17: 743,107-743,107 , GRCh38 chr17: 737,687-737,687 , GRCh37.p13 chr17: 640,927-640,927 , GRCh37.p13 chr17: 646,347-646,347 TLCD3A, GEMIN4
    nsv5344933translocation1nstd200human GRCh37 chr17: 646,347-646,347 , GRCh37 chr17: 640,927-640,927 , GRCh38.p12 chr17: 737,687-737,687 , GRCh38.p12 chr17: 743,107-743,107 TLCD3A, GEMIN4
    nsv5320901translocation1nstd204human GRCh37.p13 chr17: 640,927-640,927 , GRCh37.p13 chr17: 646,347-646,347 , GRCh38.p13 chr17: 743,107-743,107 , GRCh38.p13 chr17: 737,687-737,687 GEMIN4, TLCD3A
    nsv5310120copy number variation1nstd204human GRCh37.p13 chr17: 640,904-646,355 , GRCh38.p13 chr17: 737,664-743,115 GEMIN4, TLCD3A
    nsv5290569copy number variation1nstd204human GRCh38.p13 chr17: 737,635-743,234 , GRCh37.p13 chr17: 640,875-646,474 GEMIN4, TLCD3A
    nsv5159687mobile element insertion1nstd203human GRCh38 chr17: 744,696-744,710 , GRCh37.p13 chr17: 647,936-647,950 GEMIN4
    nsv5015231copy number variation1nstd200human GRCh38 chr17: 737,670-743,106 , GRCh37.p13 chr17: 640,910-646,346 GEMIN4, TLCD3A
    nsv5013629copy number variation1nstd200human GRCh38 chr17: 738,101-895,221 , GRCh37.p13 chr17: 641,341-798,461 GEMIN4, MRM3, 4 more genes
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