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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112696copy number variation1nstd102humanUncertain significance GRCh38 chr20: 49,212,886-49,410,642 , GRCh37.p13 chr20: 47,829,423-48,027,179 KCNB1, DDX27, 7 more genes
    nsv5953893copy number variation1nstd209human GRCh38 chr20: 49,280,820-49,283,029 , GRCh37.p13 chr20: 47,897,357-47,899,566 ZFAS1, SNORD12, 1 more genes
    nsv5953769copy number variation1nstd209human GRCh38 chr20: 49,280,395-49,280,465 , GRCh37.p13 chr20: 47,896,932-47,897,002 ZFAS1, SNORD12, 1 more genes
    nsv5293775copy number variation1nstd204human GRCh38.p13 chr20: 49,278,301-49,289,700 , GRCh37.p13 chr20: 47,894,838-47,906,237 SNORD12C, SNORD12, 3 more genes
    nsv5025681copy number variation1nstd200human GRCh38 chr20: 49,254,626-49,283,829 , GRCh37.p13 chr20: 47,871,163-47,900,366 SNORD12C, SNORD12B, 3 more genes
    nsv4865618copy number variation1nstd200human GRCh37 chr20: 47,850,715-47,897,504 , GRCh38.p12 chr20: 49,234,178-49,280,967 ZNFX1, SNORD12, 4 more genes
    nsv4681865copy number variation1nstd102humanUncertain significance GRCh37 chr20: 47,538,407-48,099,037 , GRCh38.p12 chr20: 48,921,870-49,482,500 ARFGEF2, LOC105372649, 12 more genes
    nsv4632839copy number variation1nstd183human GRCh37 chr20: 47,892,453-47,895,183 , GRCh38.p12 chr20: 49,275,916-49,278,646 ZNFX1, SNORD12C, 2 more genes
    nsv4630531copy number variation1nstd183human GRCh37 chr20: 47,894,640-47,906,255 , GRCh38.p12 chr20: 49,278,103-49,289,718 ZFAS1, SNORD12C, 3 more genes
    nsv4621478copy number variation1nstd183human GRCh37 chr20: 47,752,123-47,988,180 , GRCh38.p12 chr20: 49,135,586-49,371,643 SNORD12, STAU1, 8 more genes
    nsv3922231copy number variation1nstd102humanUncertain significance GRCh38 chr20: 49,098,782-49,465,707 , GRCh37 chr20: 47,715,319-48,082,244 , NCBI36 chr20: 47,148,726-47,515,651 ZFAS1, ZNFX1, 8 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3920108copy number variation1nstd102humanUncertain significance GRCh37 chr20: 47,373,123-48,148,892 , NCBI36 chr20: 46,806,530-47,582,299 , GRCh38 chr20: 48,756,586-49,532,355 ZFAS1, CSE1L, 14 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 RNA5SP481, LOC105372625, 855 more genes
    nsv3908507copy number variation1nstd102humanPathogenic GRCh37 chr20: 47,627,844-52,045,480 , GRCh38.p12 chr20: 49,011,307-53,428,941 LOC100419570, KCNB1, 93 more genes
    nsv3907741copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 47,726,521-50,427,649 , GRCh38.p12 chr20: 49,109,984-51,811,110 CEBPB, KCNB1, 70 more genes
    nsv3906682copy number variation1nstd102humanUncertain significance GRCh37 chr20: 47,427,610-48,085,774 , GRCh38.p12 chr20: 48,811,073-49,469,237 ZNFX1, SNAP23P1, 13 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 LRRN4, SNRPB, 1313 more genes
    nsv3896520copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110 COMMD7, RNU7-6P, 1311 more genes
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