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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4964152copy number variation1nstd200human GRCh38 chr9: 31,163,126-31,578,185 , GRCh37.p13 chr9: 31,163,124-31,578,183 SLC25A6P2, LOC105376010, 3 more genes
    nsv4964151copy number variation1nstd200human GRCh38 chr9: 31,163,127-31,563,754 , GRCh37.p13 chr9: 31,163,125-31,563,752 MTCO3P30, SLC25A6P2, 2 more genes
    nsv4954628copy number variation1nstd200human GRCh38 chr9: 31,218,861-31,396,758 , GRCh37.p13 chr9: 31,218,859-31,396,756 SLC25A6P2, LINC01243
    nsv4954627copy number variation1nstd200human GRCh38 chr9: 31,058,064-31,401,281 , GRCh37.p13 chr9: 31,058,062-31,401,279 LOC105376009, SLC25A6P2, 1 more genes
    nsv4954622copy number variation1nstd200human GRCh38 chr9: 30,391,634-31,423,819 , GRCh37.p13 chr9: 30,391,632-31,423,817 RPS26P2, KRT18P36, 11 more genes
    nsv4814730copy number variation1nstd200human GRCh37 chr9: 31,369,078-31,391,956 , GRCh38.p12 chr9: 31,369,080-31,391,958 LINC01243
    nsv4814729copy number variation1nstd200human GRCh37 chr9: 31,218,859-31,396,756 , GRCh38.p12 chr9: 31,218,861-31,396,758 SLC25A6P2, LINC01243
    nsv4814728copy number variation1nstd200human GRCh37 chr9: 31,058,062-31,401,279 , GRCh38.p12 chr9: 31,058,064-31,401,281 LOC105376009, LINC01243, 1 more genes
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4679276copy number variation1nstd189human GRCh38.p12 chr9: 31,164,392-31,562,555 , GRCh37.p13 chr9: 31,164,390-31,562,553 SLC25A6P2, LINC01243, 2 more genes
    nsv4675631copy number variation1nstd102humanUncertain significance GRCh37 chr9: 28,183,564-31,526,964 , GRCh38.p12 chr9: 28,183,566-31,526,966 LOC105376005, ME2P1, 22 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4604556copy number variation1nstd183human GRCh37 chr9: 31,172,350-31,679,894 , GRCh38.p12 chr9: 31,172,352-31,679,896 SLC25A6P2, HMGB3P23, 4 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4456028copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-38,472,979 , GRCh38.p12 chr9: 203,861-38,472,982 SNORA30B, LOC100419692, 559 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv4429561copy number variation1nstd174human GRCh37 chr9: 31,301,853-31,391,583 , GRCh38.p12 chr9: 31,301,855-31,391,585 LINC01243
    nsv4425578copy number variation1nstd174human GRCh37 chr9: 31,164,389-31,685,359 , GRCh38.p12 chr9: 31,164,391-31,685,361 SLC25A6P2, HMGB3P23, 4 more genes
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