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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5326893copy number variation1nstd204human GRCh38.p13 chr20: 47,383,910-47,527,506 , GRCh37.p13 chr20: 46,012,654-46,156,250 LINC01754, RPL35AP, 3 more genes
    nsv5299953copy number variation1nstd204human GRCh38.p13 chr20: 47,420,133-47,479,041 , GRCh37.p13 chr20: 46,048,877-46,107,785 RPL35AP
    nsv5297292copy number variation1nstd204human GRCh38.p13 chr20: 47,465,601-47,617,800 , GRCh37.p13 chr20: 46,094,345-46,246,544 RNU6-497P, RPL35AP, 2 more genes
    nsv5292479copy number variation1nstd204human GRCh37.p13 chr20: 45,897,945-46,153,944 , GRCh38.p13 chr20: 47,269,201-47,525,200 NCOA3, ZMYND8, 6 more genes
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
    nsv4620665copy number variation1nstd183human GRCh37 chr20: 45,978,466-46,365,571 , GRCh38.p12 chr20: 47,349,722-47,736,827 NCOA3, ZMYND8, 7 more genes
    nsv4536379copy number variation1nstd166human GRCh37.p13 chr20: 45,980,999-46,225,000 , GRCh38.p12 chr20: 47,352,255-47,596,256 NCOA3, ZMYND8, 5 more genes
    nsv4385888copy number variation2nstd173human GRCh37 chr20: 46,071,366-46,109,076 , GRCh38.p12 chr20: 47,442,622-47,480,332 RPL35AP
    nsv4376514copy number variation1nstd173human GRCh37 chr20: 46,077,181-46,108,458 , GRCh38.p12 chr20: 47,448,437-47,479,714 RPL35AP
    nsv3921364copy number variation1nstd102humanLikely benign GRCh38 chr20: 47,390,946-47,514,274 , NCBI36 chr20: 45,453,097-45,576,425 , GRCh37 chr20: 46,019,690-46,143,018 NCOA3, RNU6-563P, 3 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
    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
    nsv3912723copy number variation1nstd102humanPathogenic NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019 LOC107985448, LOC105372613, 370 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
    nsv3910049copy number variation1nstd102humanPathogenic NCBI36 chr20: 33,289,165-45,693,969 , GRCh37 chr20: 33,825,749-46,260,562 , GRCh38 chr20: 35,237,946-47,631,818 NDUFB4P10, EIF4EBP2P1, 291 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
    nsv3895314copy number variation2nstd102humanPathogenic GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202 PKIG, LINC01523, 1311 more genes
    nsv3892750copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941 TGIF2-RAB5IF, LOC105372609, 1314 more genes
    nsv3169101copy number variation1nstd158human GRCh37 chr20: 45,616,408-48,595,215 , GRCh38.p12 chr20: 46,987,769-49,978,678 , CSE1L, 68 more genes
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