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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098935copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,603,558-44,033,313 , GRCh37.p13 chr17: 41,680,926-42,110,681 LOC107985086, MPP2, 21 more genes
    nsv7095169copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,738,414-41,738,902 , GRCh38.p12 chr17: 43,661,046-43,661,534 MEOX1
    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
    nsv6989800copy number variation1nstd229human GRCh38 chr17: 43,658,101-43,678,400 , GRCh37.p13 chr17: 41,735,469-41,755,768 MEOX1, LINC02594, 1 more genes
    nsv6988876copy number variation1nstd229human GRCh38 chr17: 43,651,946-43,651,977 , GRCh37.p13 chr17: 41,729,314-41,729,345 MEOX1
    nsv6983326copy number variation1nstd229human GRCh38 chr17: 43,653,796-43,739,183 , GRCh37.p13 chr17: 41,731,164-41,816,551 LOC107985085, LINC02594, 2 more genes
    nsv6982907copy number variation1nstd229human GRCh38 chr17: 43,638,104-43,641,264 , GRCh37.p13 chr17: 41,715,472-41,718,632 MEOX1
    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
    nsv6499125copy number variation1nstd223human GRCh38 chr17: 43,638,994-43,639,769 , GRCh37.p13 chr17: 41,716,362-41,717,137 MEOX1
    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
    nsv6250808mobile element insertion1nstd215human GRCh38 chr17: 43,655,673-43,655,673 , GRCh37.p13 chr17: 41,733,041-41,733,041 MEOX1
    nsv5932567copy number variation1nstd209human GRCh38 chr17: 43,638,994-43,639,768 , GRCh37.p13 chr17: 41,716,362-41,717,136 MEOX1
    nsv5701526mobile element insertion1nstd211human GRCh38 chr17: 43,655,686-43,655,686 , GRCh37.p13 chr17: 41,733,054-41,733,054 MEOX1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5517243copy number variation1nstd206human GRCh38 chr17: 43,648,630-43,650,435 , GRCh37.p13 chr17: 41,725,998-41,727,803 MEOX1
    nsv5514298copy number variation1nstd206human GRCh38 chr17: 43,639,126-43,639,804 , GRCh37.p13 chr17: 41,716,494-41,717,172 MEOX1
    nsv5392965copy number variation1nstd186human GRCh37 chr17: 41,716,308-41,717,172 , GRCh38.p12 chr17: 43,638,940-43,639,804 MEOX1
    nsv5391790copy number variation1nstd186human GRCh37 chr17: 41,716,307-41,717,226 , GRCh38.p12 chr17: 43,638,939-43,639,858 MEOX1
    nsv5158743mobile element insertion1nstd203human GRCh38 chr17: 43,653,721-43,653,744 , GRCh37.p13 chr17: 41,731,089-41,731,112 MEOX1
    nsv5013730copy number variation1nstd200human GRCh38 chr17: 43,638,938-43,639,859 , GRCh37.p13 chr17: 41,716,306-41,717,227 MEOX1
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