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Items: 1 to 20 of 88

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5529572copy number variation1nstd206human GRCh38 chr20: 14,116,138-14,167,512 , GRCh37.p13 chr20: 14,096,784-14,148,158 MACROD2, AIMP1P1
    nsv5327208copy number variation1nstd204human GRCh38.p13 chr20: 13,618,297-14,410,459 , GRCh37.p13 chr20: 13,598,944-14,391,105 RPS3P1, SEL1L2, 10 more genes
    nsv5295825copy number variation1nstd204human GRCh38.p13 chr20: 13,662,701-14,410,500 , GRCh37.p13 chr20: 13,643,348-14,391,146 SEL1L2, ESF1, 9 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
    nsv4631401copy number variation1nstd183human GRCh37 chr20: 14,085,217-14,173,546 , GRCh38.p12 chr20: 14,104,571-14,192,900 MACROD2, AIMP1P1
    nsv4350090copy number variation1nstd102humanPathogenic GRCh37 chr20: 11,716,825-19,331,055 , GRCh38.p12 chr20: 11,736,177-19,350,411 ENSAP1, BANF2, 107 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
    nsv3957263copy number variation1nstd168human GRCh38 chr20: 14,097,495-14,150,878 , GRCh37.p13 chr20: 14,078,141-14,131,524 MACROD2, AIMP1P1
    nsv3922272copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103 ISM1-AS1, CST2, 498 more genes
    nsv3921972copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-19,074,923 , GRCh38 chr20: 89,939-19,146,279 , GRCh37 chr20: 70,580-19,126,923 PTMAP3, LOC105372517, 331 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
    nsv3919898copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38 chr20: 80,927-26,324,843 , NCBI36 chr20: 9,568-26,253,479 MIR3192, CFAP61, 473 more genes
    nsv3917353copy number variation1nstd102humanUncertain significance GRCh38 chr20: 9,290,612-14,648,536 , NCBI36 chr20: 9,219,259-14,577,182 , GRCh37 chr20: 9,271,259-14,629,182 LOC107985384, LOC107985407, 63 more genes
    nsv3914413copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-19,000,139 , GRCh38 chr20: 89,939-19,071,495 , GRCh37 chr20: 70,580-19,052,139 ZNF343, C20orf96, 331 more genes
    nsv3914070copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,928-18,688,031 , NCBI36 chr20: 9,569-18,616,675 , GRCh37 chr20: 61,569-18,668,675 CDC25B, LOC105372517, 324 more genes
    nsv3913796copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-28,133,653 , GRCh37.p13 chr20: 70,580-29,519,992 , GRCh38.p12 chr20: 89,939-30,285,316 RNY4P11, EIF4E2P1, 500 more genes
    nsv3913704copy number variation1nstd102humanPathogenic GRCh38 chr20: 89,939-25,697,564 , NCBI36 chr20: 18,580-25,626,200 , GRCh37 chr20: 70,580-25,678,200 NRSN2, LOC102724545, 459 more genes
    nsv3913320copy number variation1nstd102humanUncertain significance NCBI36 chr20: 12,059,236-14,616,123 , GRCh38 chr20: 12,130,588-14,687,477 , GRCh37 chr20: 12,111,236-14,668,123 SEL1L2, GAPDHP2, 26 more genes
    nsv3910142copy number variation1nstd102humanPathogenic GRCh37 chr20: 9,792,081-37,945,599 , GRCh38 chr20: 9,811,433-39,316,956 , NCBI36 chr20: 9,740,081-37,379,013 DYNLRB1, LOC107985402, 555 more genes
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