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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5283549copy number variation1nstd204human GRCh38.p13 chr20: 31,227,801-32,548,400 , GRCh37.p13 chr20: 29,815,604-31,136,202 , XKR7, 52 more genes
    nsv4681607copy number variation1nstd102humanUncertain significance GRCh37 chr20: 30,795,725-31,395,729 , GRCh38.p12 chr20: 32,207,922-32,807,923 ASXL1, MIR1825, 11 more genes
    nsv4457806copy number variation1nstd102humanPathogenic GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549 EFCAB8, C20orf203, 162 more genes
    nsv4282576copy number variation1nstd166human GRCh37.p13 chr20: 30,787,479-30,788,143 , GRCh38.p12 chr20: 32,199,676-32,200,340 PLAGL2
    nsv3963990insertion1nstd168human GRCh38 chr20: 32,197,174-32,211,712 , GRCh37.p13 chr20: 30,784,977-30,799,515 POFUT1, PLAGL2
    nsv3920503copy number variation1nstd102humanPathogenic GRCh38 chr20: 32,062,768-35,906,606 , NCBI36 chr20: 30,114,232-33,957,942 , GRCh37 chr20: 30,650,571-34,494,528 UQCC1, MIR1289-1, 111 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
    nsv3918053copy number variation1nstd102humanPathogenic NCBI36 chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426 MYH7B, PPP1R16B, 300 more genes
    nsv3917138copy number variation1nstd102humanPathogenic GRCh38 chr20: 31,254,983-33,473,080 , NCBI36 chr20: 29,306,447-31,524,547 , GRCh37 chr20: 29,842,786-32,060,886 HAUS6P2, DEFB119, 78 more genes
    nsv3912259copy number variation1nstd102humanPathogenic GRCh38 chr20: 31,254,983-32,575,288 , NCBI36 chr20: 29,306,447-30,626,751 , GRCh37 chr20: 29,842,786-31,163,090 RNA5SP482, DKKL1P1, 51 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
    nsv3910142copy number variation1nstd102humanPathogenic GRCh37 chr20: 9,792,081-37,945,599 , GRCh38 chr20: 9,811,433-39,316,956 , NCBI36 chr20: 9,740,081-37,379,013 DYNLRB1, LOC107985402, 555 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
    nsv3904899copy number variation1nstd102humanPathogenic GRCh37 chr20: 17,705,775-31,600,738 , GRCh38.p12 chr20: 17,725,130-33,012,932 TTLL9, ABHD12, 297 more genes
    nsv3897443copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 24,162,775-31,820,857 , GRCh38.p12 chr20: 24,182,139-33,233,051 BCL2L1, BAK1P1, 165 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
    nsv3878906copy number variation1nstd102humanPathogenic GRCh37 chr20: 17,705,775-31,600,738 , GRCh38.p12 chr20: 17,725,130-33,012,932 KIF3B, GINS1, 297 more genes
    nsv3168203copy number variation1nstd158human GRCh37 chr20: 2,701,906-32,918,468 , GRCh38.p12 chr20: 2,721,260-34,330,662 , ADRA1D, 557 more genes
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