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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7035396copy number variation1nstd229human GRCh38 chr20: 32,001,432-32,013,721 , GRCh37.p13 chr20: 30,589,235-30,601,524 CCM2L, RNA5SP481, 1 more genes
    nsv7032553copy number variation1nstd229human GRCh38 chr20: 31,989,868-31,989,889 , GRCh37.p13 chr20: 30,577,671-30,577,692 XKR7
    nsv7028368copy number variation1nstd229human GRCh38 chr20: 31,579,910-33,642,127 , GRCh37.p13 chr20: 30,167,713-32,229,933 PLAGL2, BPIFB4, 57 more genes
    nsv7025319copy number variation1nstd229human GRCh38 chr20: 31,987,337-32,022,524 , GRCh37.p13 chr20: 30,575,140-30,610,327 XKR7, CCM2L, 1 more genes
    nsv7022403copy number variation1nstd229human GRCh38 chr20: 31,990,386-31,990,563 , GRCh37.p13 chr20: 30,578,189-30,578,366 XKR7
    nsv7019603copy number variation1nstd229human GRCh38 chr20: 31,763,891-31,974,358 , GRCh37.p13 chr20: 30,351,694-30,562,161 PDRG1, XKR7, 6 more genes
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6637514copy number variation1nstd102humanUncertain significance GRCh37 chr20: 30,299,729-30,687,587 , GRCh38.p12 chr20: 31,711,926-32,099,784 RNA5SP482, TTLL9, 13 more genes
    nsv6531574copy number variation1nstd223human GRCh38 chr20: 31,996,690-31,998,368 , GRCh37.p13 chr20: 30,584,493-30,586,171 XKR7
    nsv6527305copy number variation1nstd223human GRCh38 chr20: 31,763,891-31,974,354 , GRCh37.p13 chr20: 30,351,694-30,562,157 TTLL9, FOXS1, 6 more genes
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 LOC105372586, RNU6-384P, 193 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6227402copy number variation1nstd214human GRCh38 chr20: 31,987,408-31,987,483 , GRCh37.p13 chr20: 30,575,211-30,575,286 XKR7
    nsv6226976copy number variation1nstd214human GRCh38 chr20: 31,986,758-31,986,809 , GRCh37.p13 chr20: 30,574,561-30,574,612 XKR7
    nsv6221268copy number variation1nstd214human GRCh38 chr20: 31,986,043-31,986,166 , GRCh37.p13 chr20: 30,573,846-30,573,969 XKR7
    nsv6216208copy number variation1nstd214human GRCh38 chr20: 31,987,028-31,987,103 , GRCh37.p13 chr20: 30,574,831-30,574,906 XKR7
    nsv6210099copy number variation1nstd214human GRCh38 chr20: 31,985,777-31,985,867 , GRCh37.p13 chr20: 30,573,580-30,573,670 XKR7
    nsv6134285copy number variation1nstd213human GRCh37 chr20: 30,240,000-30,610,001 , GRCh38.p12 chr20: 31,652,197-32,022,198 ABALON, RNU1-94P, 11 more genes
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