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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077300inversion1nstd229human GRCh38 chr20: 52,706,618-56,026,754 , GRCh37.p13 chr20: 51,323,157-54,601,810 TSHZ2, LOC105372671, 26 more genes
    nsv7075103inversion1nstd229human GRCh38 chr20: 48,844,229-55,780,453 , GRCh37.p13 chr20: 47,460,766-54,355,509 RPL12P4, LOC105372664, 113 more genes
    nsv7074277inversion1nstd229human GRCh38 chr20: 53,694,995-54,252,375 , GRCh37.p13 chr20: 52,311,534-52,868,914 BCAS1, MIR4756, 5 more genes
    nsv7072131inversion1nstd229human GRCh38 chr20: 53,548,074-57,294,874 , GRCh37.p13 chr20: 52,164,613-55,869,930 CBLN4, RNU6-1146P, 46 more genes
    nsv7071269inversion1nstd229human GRCh38 chr20: 51,579,374-58,024,568 , GRCh37.p13 chr20: 50,195,913-56,599,624 CBLN4, LOC105372693, 89 more genes
    nsv7064075inversion1nstd229human GRCh38 chr20: 49,009,324-55,851,498 , GRCh37.p13 chr20: 47,625,861-54,426,554 DPM1, KCNG1, 115 more genes
    nsv7063616inversion1nstd229human GRCh38 chr20: 51,911,434-57,961,609 , GRCh37.p13 chr20: 50,527,973-56,536,665 FAM210B, BCAS1, 81 more genes
    nsv7058989inversion1nstd229human GRCh38 chr20: 52,927,440-57,459,107 , GRCh37.p13 chr20: 51,543,979-56,034,163 FAM210B, RPS4XP3, 61 more genes
    nsv7058267inversion1nstd229human GRCh38 chr20: 51,559,821-57,992,303 , GRCh37.p13 chr20: 50,176,360-56,567,359 LOC105372683, MRPS33P4, 89 more genes
    nsv7058201inversion1nstd229human GRCh38 chr20: 51,845,371-57,066,404 , GRCh37.p13 chr20: 50,461,910-55,641,460 RNU6-347P, RPS4XP3, 61 more genes
    nsv6134307copy number variation1nstd213human GRCh37 chr20: 52,100,000-52,910,001 , GRCh38.p12 chr20: 53,483,461-54,293,462 SUMO1P1, CYP24A1, 11 more genes
    nsv6134305copy number variation1nstd213human GRCh37 chr20: 49,550,000-54,370,001 , GRCh38.p12 chr20: 50,933,463-55,794,945 KCNG1, NFATC2, 50 more genes
    nsv6134040copy number variation1nstd213human GRCh37 chr20: 51,820,000-60,870,001 , GRCh38.p12 chr20: 53,203,461-62,294,945 MC3R, PPP1R3D, 142 more genes
    nsv6133829copy number variation1nstd213human GRCh37 chr20: 51,750,000-55,610,001 , GRCh38.p12 chr20: 53,133,461-57,034,945 CASS4, FAM210B, 44 more genes
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5160174mobile element insertion1nstd203human GRCh38 chr20: 53,875,411-53,875,425 , GRCh37.p13 chr20: 52,491,950-52,491,964 SUMO1P1
    nsv5025724copy number variation1nstd200human GRCh38 chr20: 53,541,453-54,191,944 , GRCh37.p13 chr20: 52,157,992-52,808,483 BCAS1, SUMO1P1, 7 more genes
    nsv5013197copy number variation1nstd200human GRCh38 chr20: 53,874,247-53,883,339 , GRCh37.p13 chr20: 52,490,786-52,499,878 SUMO1P1
    nsv4865642copy number variation1nstd200human GRCh37 chr20: 52,157,992-52,808,483 , GRCh38.p12 chr20: 53,541,453-54,191,944 MIR4756, RNU7-14P, 7 more genes
    nsv4853922copy number variation1nstd200human GRCh37 chr20: 52,490,786-52,499,874 , GRCh38.p12 chr20: 53,874,247-53,883,335 SUMO1P1
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