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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7095881copy number variation1nstd102humanUncertain significance GRCh37 chr20: 21,686,351-21,695,441 , GRCh38.p12 chr20: 21,705,713-21,714,803 PAX1
    nsv7059744inversion1nstd229human GRCh38 chr20: 21,466,320-22,009,223 , GRCh37.p13 chr20: 21,446,958-21,989,861 SLC25A6P1, LINC01726, 7 more genes
    nsv7034029copy number variation1nstd229human GRCh38 chr20: 21,567,962-22,314,751 , GRCh37.p13 chr20: 21,548,600-22,295,389 LOC105372560, LINC01432, 7 more genes
    nsv7032944copy number variation1nstd229human GRCh38 chr20: 21,647,392-21,721,833 , GRCh37.p13 chr20: 21,628,030-21,702,471 PAX1, LINC01726
    nsv7027511copy number variation1nstd229human GRCh38 chr20: 21,460,501-21,962,500 , GRCh37.p13 chr20: 21,441,139-21,943,138 RPL41P1, PAX1, 7 more genes
    nsv7023451copy number variation1nstd229human GRCh38 chr20: 21,718,950-21,718,988 , GRCh37.p13 chr20: 21,699,588-21,699,626 PAX1
    nsv6528460copy number variation1nstd223human GRCh38 chr20: 21,567,962-22,314,751 , GRCh37.p13 chr20: 21,548,600-22,295,389 PAX1, RPL41P1, 7 more genes
    nsv6525978copy number variation1nstd223human GRCh38 chr20: 21,033,639-22,376,670 , GRCh37.p13 chr20: 21,014,280-22,357,308 LOC105372561, KIZ, 22 more genes
    nsv6314164copy number variation1nstd102humanPathogenic GRCh37 chr20: 19,292,925-22,187,397 , GRCh38.p12 chr20: 19,312,281-22,206,759 SLC25A6P1, RPL41P1, 37 more genes
    nsv6314135copy number variation1nstd102humanUncertain significance GRCh37 chr20: 21,436,009-21,984,316 , GRCh38.p12 chr20: 21,455,371-22,003,678 RPL41P1, SLC25A6P1, 7 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
    nsv6134275copy number variation1nstd213human GRCh37 chr20: 19,430,000-23,860,001 , GRCh38.p12 chr20: 19,449,356-23,879,364 CST1, CST4, 87 more genes
    nsv6134268copy number variation1nstd213human GRCh37 chr20: 13,380,000-22,450,001 , GRCh38.p12 chr20: 13,399,353-22,469,363 BFSP1, INSM1, 134 more genes
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4457709copy number variation1nstd102humanUncertain significance GRCh37 chr20: 20,817,608-21,771,865 , GRCh38.p12 chr20: 20,836,965-21,791,227 LOC112268271, RPS15AP1, 19 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    nsv4336704sequence alteration1nstd166human GRCh37.p13 chr20: 8,105,854-23,795,733 , GRCh38.p12 chr20: 8,125,207-23,815,096 , BFSP1, 242 more genes
    nsv4279779copy number variation1nstd166human GRCh37.p13 chr20: 21,698,803-21,709,701 , GRCh38.p12 chr20: 21,718,165-21,729,063 PAX1
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