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Items: 1 to 20 of 118

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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
    nsv7070199inversion1nstd229human GRCh38 chr20: 13,206,278-18,470,226 , GRCh37.p13 chr20: 13,186,925-18,450,870 LOC105372545, MACROD2, 73 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
    nsv7036426copy number variation1nstd229human GRCh38 chr20: 16,704,017-17,308,202 , GRCh37.p13 chr20: 16,684,662-17,288,847 LOC105372546, LOC105372544, 6 more genes
    nsv7031602copy number variation1nstd229human GRCh38 chr20: 14,522,099-17,023,961 , GRCh37.p13 chr20: 14,502,745-17,004,606 SNRPB2, KIF16B, 16 more genes
    nsv7031144copy number variation1nstd229human GRCh38 chr20: 16,751,009-17,002,127 , GRCh37.p13 chr20: 16,731,654-16,982,772 OTOR
    nsv6626550copy number variation1nstd224human GRCh37 chr20: 15,356,234-16,843,051 , GRCh38.p12 chr20: 15,375,589-16,862,406 KIF16B, LOC105372541, 9 more genes
    nsv6599358inversion1nstd223human GRCh38 chr20: 10,362,749-19,023,339 , GRCh37.p13 chr20: 10,343,397-19,003,983 JAG1, BFSP1, 122 more genes
    nsv6516080copy number variation1nstd223human GRCh38 chr20: 16,751,009-17,002,124 , GRCh37.p13 chr20: 16,731,654-16,982,769 OTOR
    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
    nsv5727500mobile element insertion1nstd211human GRCh38 chr20: 16,749,574-16,749,574 , GRCh37.p13 chr20: 16,730,219-16,730,219 OTOR
    nsv5530660copy number variation1nstd206human GRCh38 chr20: 16,704,017-17,308,202 , GRCh37.p13 chr20: 16,684,662-17,288,847 PCSK2, SNRPB2, 6 more genes
    nsv5192634mobile element insertion1nstd203human GRCh38 chr20: 16,749,562-16,749,574 , GRCh37.p13 chr20: 16,730,207-16,730,219 OTOR
    nsv5167623mobile element insertion1nstd203human GRCh38 chr20: 16,751,820-16,751,832 , GRCh37.p13 chr20: 16,732,465-16,732,477 OTOR
    nsv5025168copy number variation1nstd200human GRCh38 chr20: 16,751,009-17,002,129 , GRCh37.p13 chr20: 16,731,654-16,982,774 OTOR
    nsv5025167copy number variation1nstd200human GRCh38 chr20: 16,704,017-17,308,202 , GRCh37.p13 chr20: 16,684,662-17,288,847 LOC105372544, RNU6-27P, 6 more genes
    nsv4865459copy number variation1nstd200human GRCh37 chr20: 16,684,662-17,288,847 , GRCh38.p12 chr20: 16,704,017-17,308,202 LOC105372545, LOC105372544, 6 more genes
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