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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972935insertion1nstd209human GRCh38 chr20: 46,726,620-46,726,620 , GRCh37.p13 chr20: 45,355,259-45,355,259 SLC2A10
    nsv5550747insertion1nstd206human GRCh38 chr20: 46,727,566-46,727,606 , GRCh37.p13 chr20: 45,356,205-45,356,245 SLC2A10
    nsv5524570copy number variation1nstd206human GRCh38 chr20: 46,735,140-46,735,798 , GRCh37.p13 chr20: 45,363,779-45,364,437 SLC2A10
    nsv5520269copy number variation1nstd206human GRCh38 chr20: 46,726,549-46,726,635 , GRCh37.p13 chr20: 45,355,188-45,355,274 SLC2A10
    nsv5381081copy number variation1nstd102humanUncertain significance GRCh37 chr20: 45,362,375-45,362,493 , GRCh38.p12 chr20: 46,733,736-46,733,854 SLC2A10
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
    nsv4578512copy number variation1nstd102humannot provided GRCh37 chr20: 45,356,083-45,358,404 , GRCh38 chr20: 46,727,444-46,729,765 SLC2A10
    nsv4534379copy number variation1nstd166human GRCh37.p13 chr20: 45,298,999-45,383,000 , GRCh38.p12 chr20: 46,670,360-46,754,361 SLC2A10, TP53RK, 1 more genes
    nsv4457837copy number variation1nstd102humanUncertain significance GRCh37 chr20: 45,350,682-45,499,090 , GRCh38.p12 chr20: 46,722,043-46,870,451 RN7SKP33, SLC2A10, 1 more genes
    nsv4283932copy number variation1nstd166human GRCh37.p13 chr20: 45,300,376-45,337,781 , GRCh38.p12 chr20: 46,671,737-46,709,142 TP53RK, SLC13A3, 1 more genes
    nsv4282578copy number variation1nstd166human GRCh37.p13 chr20: 45,298,296-45,383,847 , GRCh38.p12 chr20: 46,669,657-46,755,208 SLC2A10, SLC13A3, 1 more genes
    nsv4282462copy number variation1nstd166human GRCh37.p13 chr20: 45,361,795-45,365,680 , GRCh38.p12 chr20: 46,733,156-46,737,041 SLC2A10
    nsv4282442copy number variation1nstd166human GRCh37.p13 chr20: 45,362,359-45,380,424 , GRCh38.p12 chr20: 46,733,720-46,751,785 SLC2A10
    nsv4273815copy number variation1nstd166human GRCh37.p13 chr20: 45,355,188-45,355,274 , GRCh38.p12 chr20: 46,726,549-46,726,635 SLC2A10
    nsv3959357copy number variation1nstd168human GRCh38 chr20: 46,724,109-46,735,181 , GRCh37.p13 chr20: 45,352,748-45,363,820 SLC2A10
    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
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 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
    nsv3910049copy number variation1nstd102humanPathogenic NCBI36 chr20: 33,289,165-45,693,969 , GRCh37 chr20: 33,825,749-46,260,562 , GRCh38 chr20: 35,237,946-47,631,818 NDUFB4P10, EIF4EBP2P1, 291 more genes
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