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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4285254copy number variation1nstd166human GRCh37.p13 chr20: 48,658,540-48,672,914 , GRCh38.p12 chr20: 50,042,003-50,056,377 TRERNA1, LOC105372655
    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
    nsv3918469copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 48,039,067-49,545,590 , GRCh37 chr20: 48,605,660-50,112,183 , GRCh38 chr20: 49,989,123-51,495,645 CEBPB, KCNG1, 40 more genes
    nsv3916972copy number variation1nstd102humanPathogenic GRCh38 chr20: 49,947,237-55,875,406 , NCBI36 chr20: 47,997,181-53,883,869 , GRCh37 chr20: 48,563,774-54,450,462 UBE2V1, KRT18P4, 87 more genes
    nsv3915867copy number variation1nstd102humanPathogenic GRCh37 chr20: 48,347,613-49,819,103 , GRCh38 chr20: 49,731,076-51,202,566 , NCBI36 chr20: 47,781,020-49,252,510 PEDS1-UBE2V1, SLC9A8, 48 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
    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
    nsv3874236copy number variation1nstd102humanUncertain significance GRCh37 chr20: 46,962,638-50,647,699 , GRCh38.p12 chr20: 48,333,895-52,031,160 MIR645, ARFGEF2, 85 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
    nsv3166993copy number variation1nstd151human GRCh37 chr20: 47,244,083-48,747,489 , GRCh38.p12 chr20: 48,627,545-50,130,952 , STAU1, 38 more genes
    nsv3164990copy number variation1nstd151human GRCh37 chr20: 47,244,083-49,520,538 , GRCh38.p12 chr20: 48,627,545-50,904,001 , CSE1L, 62 more genes
    nsv3164672copy number variation1nstd151human GRCh37 chr20: 47,245,984-48,741,721 , GRCh38.p12 chr20: 48,629,446-50,125,184 , CSE1L, 38 more genes
    nsv3163542copy number variation1nstd151human GRCh37 chr20: 48,160,839-49,212,805 , GRCh38.p12 chr20: 49,544,302-50,596,268 CEBPB, B4GALT5, 38 more genes
    nsv3159087copy number variation1nstd151human GRCh37 chr20: 47,605,025-48,700,796 , GRCh38.p12 chr20: 48,988,488-50,084,259 CSE1L, PTGIS, 35 more genes
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