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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5728067mobile element insertion2nstd211human GRCh38 chr20: 35,289,518-35,289,518 , GRCh37.p13 chr20: 33,877,321-33,877,321 FAM83C
    nsv5198518mobile element insertion1nstd203human GRCh38 chr20: 35,289,508-35,289,518 , GRCh37.p13 chr20: 33,877,311-33,877,321 FAM83C
    nsv5190969mobile element insertion1nstd203human GRCh38 chr20: 35,289,507-35,289,518 , GRCh37.p13 chr20: 33,877,310-33,877,321 FAM83C
    nsv5183801mobile element insertion1nstd203human GRCh38 chr20: 35,289,503-35,289,518 , GRCh37.p13 chr20: 33,877,306-33,877,321 FAM83C
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4868696copy number variation1nstd200human GRCh37 chr20: 33,874,227-33,877,336 , GRCh38.p12 chr20: 35,286,424-35,289,533 FAM83C
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4868578copy number variation1nstd200human GRCh37 chr20: 30,804,017-43,610,372 , GRCh38.p12 chr20: 32,216,214-44,981,731 , SNORA71C, 279 more genes
    nsv4573920mobile element insertion1nstd166human GRCh37.p13 chr20: 33,877,306-33,877,306 , GRCh38.p12 chr20: 35,289,503-35,289,503 FAM83C
    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
    nsv4279737copy number variation1nstd166human GRCh37.p13 chr20: 33,873,145-33,873,214 , GRCh38.p12 chr20: 35,285,342-35,285,411 FAM83C, FAM83C-AS1
    nsv3920503copy number variation1nstd102humanPathogenic GRCh38 chr20: 32,062,768-35,906,606 , NCBI36 chr20: 30,114,232-33,957,942 , GRCh37 chr20: 30,650,571-34,494,528 UQCC1, MIR1289-1, 111 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3918053copy number variation1nstd102humanPathogenic NCBI36 chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426 MYH7B, PPP1R16B, 300 more genes
    nsv3913986copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 33,103,319-33,489,663 , GRCh37 chr20: 33,639,658-34,026,249 , GRCh38 chr20: 35,051,855-35,438,457 EIF6, GDF5, 12 more genes
    nsv3913594copy number variation1nstd102humanPathogenic GRCh37 chr20: 32,020,169-35,450,284 , NCBI36 chr20: 31,483,830-34,883,698 , GRCh38 chr20: 33,432,363-36,821,881 AHCY, RALY, 93 more genes
    nsv3912723copy number variation1nstd102humanPathogenic NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019 LOC107985448, LOC105372613, 370 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 RNA5SP481, LOC105372625, 855 more genes
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