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Items: 1 to 20 of 398

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7037648copy number variation1nstd229human GRCh38 chr20: 35,400,701-35,428,600 , GRCh37.p13 chr20: 33,988,504-34,016,397 UQCC1
    nsv7037621copy number variation1nstd229human GRCh38 chr20: 35,383,403-35,387,147 , GRCh37.p13 chr20: 33,971,206-33,974,950 UQCC1
    nsv7033281copy number variation1nstd229human GRCh38 chr20: 35,406,391-35,409,745 , GRCh37.p13 chr20: 33,994,194-33,997,548 UQCC1
    nsv7032731copy number variation1nstd229human GRCh38 chr20: 35,402,301-35,429,300 , GRCh37.p13 chr20: 33,990,104-34,017,099 UQCC1
    nsv7032520copy number variation1nstd229human GRCh38 chr20: 35,379,071-35,383,981 , GRCh37.p13 chr20: 33,966,874-33,971,784 UQCC1
    nsv7031303copy number variation1nstd229human GRCh38 chr20: 35,348,079-35,351,165 , GRCh37.p13 chr20: 33,935,882-33,938,968 UQCC1
    nsv7029317copy number variation1nstd229human GRCh38 chr20: 35,309,417-35,315,871 , GRCh37.p13 chr20: 33,897,220-33,903,674 UQCC1
    nsv7028352copy number variation1nstd229human GRCh38 chr20: 35,276,913-35,341,707 , GRCh37.p13 chr20: 33,864,716-33,929,510 MMP24-AS1-EDEM2, EIF6, 5 more genes
    nsv7028185copy number variation1nstd229human GRCh38 chr20: 35,400,084-35,404,122 , GRCh37.p13 chr20: 33,987,887-33,991,925 UQCC1
    nsv7027120copy number variation1nstd229human GRCh38 chr20: 35,400,501-35,410,700 , GRCh37.p13 chr20: 33,988,304-33,998,503 UQCC1
    nsv7022276copy number variation1nstd229human GRCh38 chr20: 35,278,350-35,335,292 , GRCh37.p13 chr20: 33,866,153-33,923,095 MMP24-AS1-EDEM2, FAM83C-AS1, 4 more genes
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7020450copy number variation1nstd229human GRCh38 chr20: 35,309,401-35,315,800 , GRCh37.p13 chr20: 33,897,204-33,903,603 UQCC1
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6599075inversion1nstd223human GRCh38 chr20: 35,371,336-35,372,184 , GRCh37.p13 chr20: 33,959,139-33,959,987 UQCC1
    nsv6597974inversion1nstd223human GRCh38 chr20: 35,348,922-35,349,718 , GRCh37.p13 chr20: 33,936,725-33,937,521 UQCC1
    nsv6597683inversion1nstd223human GRCh38 chr20: 35,388,466-35,389,084 , GRCh37.p13 chr20: 33,976,269-33,976,887 UQCC1
    nsv6596809inversion1nstd223human GRCh38 chr20: 35,388,133-35,388,928 , GRCh37.p13 chr20: 33,975,936-33,976,731 UQCC1
    nsv6535571copy number variation1nstd223human GRCh38 chr20: 35,400,788-35,401,907 , GRCh37.p13 chr20: 33,988,591-33,989,710 UQCC1
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