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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 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
    nsv4284644copy number variation1nstd166human GRCh37.p13 chr20: 44,526,076-44,526,445 , GRCh38.p12 chr20: 45,897,437-45,897,806 PLTP, CTSA
    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
    nsv3915062delins1nstd102humanUncertain significance GRCh37 chr20: 44,520,238-44,520,263 , GRCh38 chr20: 45,891,599-45,891,624 CTSA, NEURL2
    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
    nsv3168590copy number variation1nstd158human GRCh37 chr20: 44,356,808-44,530,786 , GRCh38.p12 chr20: 45,728,169-45,902,147 PLTP, CTSA, 13 more genes
    nsv3167979copy number variation1nstd158human GRCh37 chr20: 10,950,814-51,076,738 , GRCh38.p12 chr20: 10,970,166-52,460,199 , ADA, 850 more genes
    nsv3167670copy number variation1nstd151human GRCh37 chr20: 44,108,510-44,879,938 , GRCh38.p12 chr20: 45,479,870-46,251,299 , MMP9, 44 more genes
    nsv3167246copy number variation1nstd151human GRCh37 chr20: 44,108,510-46,307,553 , GRCh38.p12 chr20: 45,479,870-47,678,809 , TNNC2, 72 more genes
    nsv3167041copy number variation1nstd151human GRCh37 chr20: 44,517,394-44,536,399 , GRCh38.p12 chr20: 45,888,755-45,907,760 CTSA, NEURL2, 2 more genes
    nsv3166786copy number variation1nstd151human GRCh37 chr20: 44,166,600-44,575,810 , GRCh38.p12 chr20: 45,537,961-45,947,171 SPATA25, HNRNPA1P3, 32 more genes
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