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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5694502mobile element insertion1nstd211human GRCh38 chr20: 45,182,807-45,182,807 , GRCh37.p13 chr20: 43,811,448-43,811,448 LINC02597
    nsv5526163copy number variation1nstd206human GRCh38 chr20: 45,184,495-45,184,823 , GRCh37.p13 chr20: 43,813,136-43,813,464 LINC02597
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5322626copy number variation1nstd204human GRCh38.p13 chr20: 45,184,465-45,184,846 , GRCh37.p13 chr20: 43,813,106-43,813,487 LINC02597
    nsv5187250mobile element insertion1nstd203human GRCh38 chr20: 45,185,253-45,185,273 , GRCh37.p13 chr20: 43,813,894-43,813,914 LINC02597
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5012829copy number variation1nstd200human GRCh38 chr20: 45,183,270-45,193,789 , GRCh37.p13 chr20: 43,811,911-43,822,430 LINC02597
    nsv4884257inversion1nstd200human GRCh37 chr20: 35,583,656-44,214,103 , GRCh38.p12 chr20: 36,955,253-45,585,464 , TGM2, 180 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
    nsv4509710mobile element insertion1nstd166human GRCh37.p13 chr20: 43,819,927-43,819,927 , GRCh38.p12 chr20: 45,191,286-45,191,286 LINC02597
    nsv4284131copy number variation1nstd166human GRCh37.p13 chr20: 43,811,911-43,822,430 , GRCh38.p12 chr20: 45,183,270-45,193,789 LINC02597
    nsv4282255copy number variation1nstd166human GRCh37.p13 chr20: 43,807,298-43,816,500 , GRCh38.p12 chr20: 45,178,657-45,187,859 LINC02597
    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
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