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Items: 1 to 20 of 108

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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
    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
    nsv7026419copy number variation1nstd229human GRCh38 chr20: 31,939,628-31,963,282 , GRCh37.p13 chr20: 30,527,431-30,551,085 PDRG1, TTLL9
    nsv7023172copy number variation1nstd229human GRCh38 chr20: 31,938,603-31,949,358 , GRCh37.p13 chr20: 30,526,406-30,537,161 TTLL9, PDRG1
    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
    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
    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
    nsv6133805copy number variation1nstd213human GRCh37 chr20: 30,440,000-30,730,001 , GRCh38.p12 chr20: 31,852,197-32,142,198 TTLL9, XKR7, 8 more genes
    nsv5283549copy number variation1nstd204human GRCh38.p13 chr20: 31,227,801-32,548,400 , GRCh37.p13 chr20: 29,815,604-31,136,202 , XKR7, 52 more genes
    nsv5022319copy number variation1nstd200human GRCh38 chr20: 31,913,474-31,952,595 , GRCh37.p13 chr20: 30,501,277-30,540,398 PDRG1, TTLL9
    nsv4632642copy number variation1nstd183human GRCh37 chr20: 29,835,049-30,626,430 , GRCh38.p12 chr20: 31,247,246-32,038,627 DEFB122, HAUS6P2, 38 more genes
    nsv4457806copy number variation1nstd102humanPathogenic GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549 EFCAB8, C20orf203, 162 more genes
    nsv4414329copy number variation1nstd174human GRCh37 chr20: 29,835,037-30,621,271 , GRCh38.p12 chr20: 31,247,234-32,033,468 CD24P3, DEFB118, 38 more genes
    nsv4291376copy number variation1nstd166human GRCh37.p13 chr20: 30,539,327-30,539,380 , GRCh38.p12 chr20: 31,951,524-31,951,577 PDRG1
    nsv3922338copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 29,297,047-30,068,749 , GRCh37 chr20: 29,833,386-30,605,088 , GRCh38 chr20: 31,245,583-32,017,285 BCL2L1, CD24P3, 38 more genes
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