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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098731copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,221,355-41,380,248 , GRCh38.p12 chr17: 43,069,338-43,228,197 BRCA1, NBR1, 7 more genes
    nsv7063144inversion1nstd229human GRCh38 chr17: 43,056,575-43,218,735 , GRCh37.p13 chr17: 41,208,592-41,370,754 NBR2, HMGN1P29, 6 more genes
    nsv6995867copy number variation1nstd229human GRCh38 chr17: 43,186,473-43,442,668 , GRCh37.p13 chr17: 41,338,490-41,520,036 RNU6-1137P, CCDC200, 8 more genes
    nsv6991508copy number variation1nstd229human GRCh38 chr17: 42,821,629-43,873,068 , GRCh37.p13 chr17: 40,973,647-41,950,436 RND2, LOC107985077, 50 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
    nsv6981860copy number variation1nstd229human GRCh38 chr17: 43,082,682-43,532,646 , GRCh37.p13 chr17: 41,234,699-41,610,014 MIR2117HG, RNU6-1137P, 20 more genes
    nsv6577078inversion1nstd223human GRCh38 chr17: 43,214,812-43,220,310 , GRCh37.p13 chr17: 41,366,831-41,372,330 CCDC200, TMEM106A
    nsv6314057copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,202,796-41,974,964 , GRCh38.p12 chr17: 43,050,779-43,897,596 TMEM106A, MPP2, 33 more genes
    nsv6133246copy number variation1nstd213human GRCh37 chr17: 40,670,000-41,570,001 , GRCh38.p12 chr17: 42,517,982-43,492,633 AOC2, ARL4D, 65 more genes
    nsv5945651copy number variation1nstd209human GRCh38 chr17: 43,216,585-43,216,691 , GRCh37.p13 chr17: 41,368,604-41,368,710 TMEM106A
    nsv5936586copy number variation1nstd209human GRCh38 chr17: 43,212,392-43,213,017 , GRCh37.p13 chr17: 41,364,411-41,365,036 TMEM106A
    nsv5936437copy number variation1nstd209human GRCh38 chr17: 43,215,940-43,216,446 , GRCh37.p13 chr17: 41,367,959-41,368,465 TMEM106A
    nsv5928779copy number variation1nstd209human GRCh38 chr17: 43,217,312-43,217,679 , GRCh37.p13 chr17: 41,369,331-41,369,698 TMEM106A
    nsv5870677copy number variation1nstd209human GRCh38 chr17: 43,217,486-43,219,685 , GRCh37.p13 chr17: 41,369,505-41,371,704 CCDC200, TMEM106A
    nsv5868736copy number variation1nstd209human GRCh38 chr17: 43,214,837-43,216,136 , GRCh37.p13 chr17: 41,366,856-41,368,155 TMEM106A
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5289818copy number variation1nstd204human GRCh38.p13 chr17: 43,159,701-43,231,500 , GRCh37.p13 chr17: 41,311,718-41,383,489 CCDC200, LOC101929767, 3 more genes
    nsv5288617copy number variation1nstd204human GRCh38.p13 chr17: 43,204,704-43,215,136 , GRCh37.p13 chr17: 41,356,721-41,367,155 TMEM106A, NBR1
    nsv5288516copy number variation1nstd204human GRCh38.p13 chr17: 43,219,661-43,233,386 , GRCh37.p13 chr17: 41,371,680-41,383,489 TMEM106A, RNU2-1, 1 more genes
    nsv5287669copy number variation1nstd204human GRCh38.p13 chr17: 42,963,201-43,231,700 , GRCh37.p13 chr17: 41,115,218-41,383,489 PTGES3L, CCDC200, 15 more genes
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