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Items: 1 to 20 of 142

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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
    nsv7098816copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 3,005,123-5,547,871 , GRCh38.p12 chr20: 3,024,477-5,567,225 ADRA1D, AVP, 70 more genes
    nsv7095879copy number variation2nstd102humanUncertain significance GRCh37 chr20: 1,959,939-6,760,201 , GRCh38.p12 chr20: 1,979,293-6,779,554 SLC23A2, TARDBPP1, 120 more genes
    nsv7063954inversion1nstd229human GRCh38 chr20: 3,693,712-5,966,241 , GRCh37.p13 chr20: 3,674,359-5,946,887 GPCPD1, PANK2, 52 more genes
    nsv7063264inversion1nstd229human GRCh38 chr20: 5,408,131-5,833,273 , GRCh37.p13 chr20: 5,388,777-5,813,919 RPS18P1, LOC643406, 8 more genes
    nsv7063012inversion1nstd229human GRCh38 chr20: 5,360,837-5,792,198 , GRCh37.p13 chr20: 5,341,483-5,772,844 RPS18P1, LOC107985411, 8 more genes
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7060087inversion1nstd229human GRCh38 chr20: 5,513,910-5,805,219 , GRCh37.p13 chr20: 5,494,556-5,785,865 SHLD1, LOC105372514, 3 more genes
    nsv7015435copy number variation1nstd229human GRCh38 chr20: 4,445,183-5,667,683 , GRCh37.p13 chr20: 4,425,830-5,648,329 LOC107985411, LOC105372510, 26 more genes
    nsv7015076copy number variation1nstd229human GRCh38 chr20: 5,542,196-5,804,666 , GRCh37.p13 chr20: 5,522,842-5,785,312 EIF4EP1, SHLD1, 2 more genes
    nsv7013247copy number variation1nstd229human GRCh38 chr20: 5,408,898-5,641,138 , GRCh37.p13 chr20: 5,389,544-5,621,784 LOC643406, LINC01729, 6 more genes
    nsv7012902copy number variation1nstd229human GRCh38 chr20: 5,466,465-5,717,830 , GRCh37.p13 chr20: 5,447,111-5,698,476 LINC01729, RPS18P1, 6 more genes
    nsv7011709copy number variation1nstd229human GRCh38 chr20: 5,493,038-5,939,581 , GRCh37.p13 chr20: 5,473,684-5,920,227 LINC00654, EIF4EP1, 9 more genes
    nsv7011702copy number variation1nstd229human GRCh38 chr20: 5,462,243-5,827,773 , GRCh37.p13 chr20: 5,442,889-5,808,419 LINC00654, GPCPD1, 7 more genes
    nsv7010990copy number variation1nstd229human GRCh38 chr20: 5,460,102-5,719,171 , GRCh37.p13 chr20: 5,440,748-5,699,817 EIF4EP1, GPCPD1, 6 more genes
    nsv7010724copy number variation1nstd229human GRCh38 chr20: 5,351,177-5,818,572 , GRCh37.p13 chr20: 5,331,823-5,799,218 EIF4EP1, GPCPD1, 8 more genes
    nsv7008977copy number variation1nstd229human GRCh38 chr20: 4,351,306-5,587,282 , GRCh37.p13 chr20: 4,331,953-5,567,928 LINC00658, GPCPD1, 26 more genes
    nsv7006847copy number variation1nstd229human GRCh38 chr20: 5,360,624-8,409,137 , GRCh37.p13 chr20: 5,341,270-8,389,784 TMX4, LINC00654, 38 more genes
    nsv7006489copy number variation1nstd229human GRCh38 chr20: 5,512,739-5,842,425 , GRCh37.p13 chr20: 5,493,385-5,823,071 GPCPD1, EIF4EP1, 3 more genes
    nsv7005541copy number variation1nstd229human GRCh38 chr20: 5,467,288-5,718,843 , GRCh37.p13 chr20: 5,447,934-5,699,489 EIF4EP1, LINC00654, 6 more genes
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