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Items: 1 to 20 of 162

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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
    nsv7095546copy number variation1nstd102humanPathogenic GRCh37 chr20: 17,587,682-18,168,103 , GRCh38.p12 chr20: 17,607,037-18,187,459 SNX5, PET117, 14 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
    nsv7070199inversion1nstd229human GRCh38 chr20: 13,206,278-18,470,226 , GRCh37.p13 chr20: 13,186,925-18,450,870 LOC105372545, MACROD2, 73 more genes
    nsv7068814inversion1nstd229human GRCh38 chr20: 17,693,112-17,695,520 , GRCh37.p13 chr20: 17,673,757-17,676,165 BANF2
    nsv7068244inversion1nstd229human GRCh38 chr20: 17,080,202-18,490,897 , GRCh37.p13 chr20: 17,060,847-18,471,541 DSTN, RNU2-56P, 42 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
    nsv7027462copy number variation1nstd229human GRCh38 chr20: 17,723,417-17,791,972 , GRCh37.p13 chr20: 17,704,062-17,772,617 BANF2
    nsv7020606copy number variation1nstd229human GRCh38 chr20: 17,700,829-17,703,282 , GRCh37.p13 chr20: 17,681,474-17,683,927 BANF2
    nsv6599358inversion1nstd223human GRCh38 chr20: 10,362,749-19,023,339 , GRCh37.p13 chr20: 10,343,397-19,003,983 JAG1, BFSP1, 122 more genes
    nsv6595708inversion1nstd223human GRCh38 chr20: 17,694,612-17,695,407 , GRCh37.p13 chr20: 17,675,257-17,676,052 BANF2
    nsv6531236copy number variation1nstd223human GRCh38 chr20: 17,697,143-17,725,637 , GRCh37.p13 chr20: 17,677,788-17,706,282 BANF2, LOC105372547
    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
    nsv6134272copy number variation1nstd213human GRCh37 chr20: 17,130,000-18,000,001 , GRCh38.p12 chr20: 17,149,355-18,019,357 BFSP1, PCSK2, 20 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
    nsv5697770mobile element insertion2nstd211human GRCh38 chr20: 17,731,781-17,731,781 , GRCh37.p13 chr20: 17,712,426-17,712,426 BANF2
    nsv5557937sequence alteration1nstd206human GRCh38 chr20: 17,701,586-17,702,011 , GRCh37.p13 chr20: 17,682,231-17,682,656 BANF2
    nsv5545930insertion1nstd206human GRCh38 chr20: 17,701,998-17,701,998 , GRCh37.p13 chr20: 17,682,643-17,682,643 BANF2
    nsv5025172copy number variation1nstd200human GRCh38 chr20: 17,723,417-17,791,972 , GRCh37.p13 chr20: 17,704,062-17,772,617 BANF2
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