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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077306inversion1nstd229human GRCh38 chr16: 20,312,926-20,501,990 , GRCh37.p13 chr16: 20,324,248-20,513,312 GP2, ACSM5, 4 more genes
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7073570inversion1nstd229human GRCh38 chr16: 20,388,212-20,388,229 , GRCh37.p13 chr16: 20,399,534-20,399,551 PDILT
    nsv7068933inversion1nstd229human GRCh38 chr16: 20,325,688-20,609,015 , GRCh37.p13 chr16: 20,337,010-20,620,337 GP2, PDILT, 9 more genes
    nsv7066661inversion1nstd229human GRCh38 chr16: 20,371,339-20,376,130 , GRCh37.p13 chr16: 20,382,661-20,387,452 PDILT
    nsv7061433inversion1nstd229human GRCh38 chr16: 19,893,387-21,501,582 , GRCh37.p13 chr16: 19,904,709-21,512,903 CRYM, SNX29P1, 38 more genes
    nsv7059443inversion1nstd229human GRCh38 chr16: 20,327,016-20,536,162 , GRCh37.p13 chr16: 20,338,338-20,547,484 ACSM2A, PDILT, 5 more genes
    nsv7059273inversion1nstd229human GRCh38 chr16: 20,380,547-20,567,019 , GRCh37.p13 chr16: 20,391,869-20,578,341 ACSM5, PDILT, 3 more genes
    nsv7059025inversion1nstd229human GRCh38 chr16: 20,379,226-20,476,570 , GRCh37.p13 chr16: 20,390,548-20,487,892 ACSM5, ACSM2A, 2 more genes
    nsv6995976copy number variation1nstd229human GRCh38 chr16: 20,377,801-20,386,200 , GRCh37.p13 chr16: 20,389,123-20,397,522 PDILT
    nsv6987458copy number variation1nstd229human GRCh38 chr16: 20,401,005-20,404,318 , GRCh37.p13 chr16: 20,412,327-20,415,640 PDILT
    nsv6983099copy number variation1nstd229human GRCh38 chr16: 20,364,262-20,367,297 , GRCh37.p13 chr16: 20,375,584-20,378,619 PDILT
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6623569copy number variation1nstd224human GRCh37 chr16: 20,164,647-20,396,057 , GRCh38.p12 chr16: 20,153,325-20,384,735 GP2, UMOD, 4 more genes
    nsv6588635inversion1nstd223human GRCh38 chr16: 20,380,562-20,381,483 , GRCh37.p13 chr16: 20,391,884-20,392,805 PDILT
    nsv6576750inversion1nstd223human GRCh38 chr16: 20,380,351-20,381,589 , GRCh37.p13 chr16: 20,391,673-20,392,911 PDILT
    nsv6514655copy number variation1nstd223human GRCh38 chr16: 20,364,260-20,367,296 , GRCh37.p13 chr16: 20,375,582-20,378,618 PDILT
    nsv6500091copy number variation1nstd223human GRCh38 chr16: 20,397,078-20,405,902 , GRCh37.p13 chr16: 20,408,400-20,417,224 PDILT
    nsv6498102copy number variation1nstd223human GRCh38 chr16: 20,376,419-20,381,052 , GRCh37.p13 chr16: 20,387,741-20,392,374 PDILT
    nsv6250147mobile element insertion1nstd215human GRCh38 chr16: 20,372,520-20,372,520 , GRCh37.p13 chr16: 20,383,842-20,383,842 PDILT
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