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Items: 1 to 20 of 107

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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
    nsv7073551inversion1nstd229human GRCh38 chr20: 10,362,744-19,023,342 , GRCh37.p13 chr20: 10,343,392-19,003,986 SLX4IP, RPL15P1, 122 more genes
    nsv7065399inversion1nstd229human GRCh38 chr20: 13,871,578-20,212,622 , GRCh37.p13 chr20: 13,852,224-20,193,266 SLC24A3, LOC107985418, 92 more genes
    nsv7035008copy number variation1nstd229human GRCh38 chr20: 18,230,215-19,166,674 , GRCh37.p13 chr20: 18,210,859-19,147,318 RN7SL14P, LOC107985418, 29 more genes
    nsv7030410copy number variation1nstd229human GRCh38 chr20: 18,365,152-18,645,606 , GRCh37.p13 chr20: 18,345,796-18,626,250 LINC00851, RNU6ATAC34P, 13 more genes
    nsv7019631copy number variation1nstd229human GRCh38 chr20: 18,510,081-18,566,620 , GRCh37.p13 chr20: 18,490,725-18,547,264 SEC23B, SMIM26
    nsv6599358inversion1nstd223human GRCh38 chr20: 10,362,749-19,023,339 , GRCh37.p13 chr20: 10,343,397-19,003,983 JAG1, BFSP1, 122 more genes
    nsv6597766inversion1nstd223human GRCh38 chr20: 18,569,573-18,570,687 , GRCh37.p13 chr20: 18,550,217-18,551,331 SMIM26
    nsv6529430copy number variation1nstd223human GRCh38 chr20: 18,365,150-18,645,606 , GRCh37.p13 chr20: 18,345,794-18,626,250 SMIM26, RPL21P3, 13 more genes
    nsv6290339copy number variation1nstd102humanUncertain significance GRCh37 chr20: 11,702,911-19,179,706 , GRCh38.p12 chr20: 11,722,263-19,199,062 LOC105372530, MACROD2-AS1, 105 more genes
    nsv6134271copy number variation1nstd213human GRCh37 chr20: 15,280,000-18,930,001 , GRCh38.p12 chr20: 15,299,354-18,949,357 PTMAP3, SEC23B, 66 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
    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
    nsv4634280copy number variation1nstd183human GRCh37 chr20: 18,208,790-19,102,422 , GRCh38.p12 chr20: 18,228,146-19,121,778 , RNA5SP476, 30 more genes
    nsv4457833copy number variation1nstd102humanUncertain significance GRCh37 chr20: 18,326,965-18,735,636 , GRCh38.p12 chr20: 18,346,321-18,754,992 DTD1-AS1, RNU6ATAC34P, 16 more genes
    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
    nsv4288638copy number variation1nstd166human GRCh37.p13 chr20: 18,490,743-18,547,264 , GRCh38.p12 chr20: 18,510,099-18,566,620 SEC23B, SMIM26
    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
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