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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv3164990copy number variation1nstd151human GRCh37 chr20: 47,244,083-49,520,538 , GRCh38.p12 chr20: 48,627,545-50,904,001 , CSE1L, 62 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
    nsv2787492copy number variation1nstd132human NCBI36 chr20: 47,690,212-48,520,857 , GRCh37.p13 chr20: 48,256,805-49,087,450 , GRCh38.p12 chr20: 49,640,268-50,470,913 CEBPB, SLC9A8, 30 more genes
    esv4007196copy number variation1estd231human GRCh37 chr20: 48,609,465-49,424,701 , GRCh38.p12 chr20: 49,992,928-50,808,164 PEDS1-UBE2V1, MIR1302-5, 26 more genes
    nsv2111512short tandem repeat1nstd128human GRCh37 chr20: 48,809,057-48,809,077 , GRCh38.p12 chr20: 50,192,520-50,192,540 CEBPB-AS1, CEBPB
    nsv2111511short tandem repeat2nstd128human GRCh37 chr20: 48,808,765-48,808,783 , GRCh38.p12 chr20: 50,192,228-50,192,246 CEBPB, CEBPB-AS1
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