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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145098insertion1nstd232human GRCh37.p13 chr20: 30,385,317-30,385,317 , GRCh38.p12 chr20: 31,797,514-31,797,514 TPX2
    nsv7139040insertion1nstd232human GRCh37.p13 chr20: 30,327,426-30,327,426 , GRCh38.p12 chr20: 31,739,623-31,739,623 TPX2
    nsv7076676inversion1nstd229human GRCh38 chr20: 31,737,021-31,737,494 , GRCh37.p13 chr20: 30,324,824-30,325,297 TPX2
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7037901copy number variation1nstd229human GRCh38 chr20: 31,423,301-31,739,500 , GRCh37.p13 chr20: 30,011,104-30,327,303 BCL2L1, DEFB123, 18 more genes
    nsv7035649copy number variation1nstd229human GRCh38 chr20: 31,764,121-31,764,168 , GRCh37.p13 chr20: 30,351,924-30,351,971 TPX2
    nsv7033753copy number variation1nstd229human GRCh38 chr20: 31,773,353-31,773,436 , GRCh37.p13 chr20: 30,361,156-30,361,239 TPX2
    nsv7028368copy number variation1nstd229human GRCh38 chr20: 31,579,910-33,642,127 , GRCh37.p13 chr20: 30,167,713-32,229,933 PLAGL2, BPIFB4, 57 more genes
    nsv7025136copy number variation1nstd229human GRCh38 chr20: 31,456,221-31,905,173 , GRCh37.p13 chr20: 30,044,024-30,492,976 COX4I2, CD24P3, 21 more genes
    nsv7020692copy number variation1nstd229human GRCh38 chr20: 31,713,834-31,791,445 , GRCh37.p13 chr20: 30,301,637-30,379,248 BCL2L1, TPX2, 2 more genes
    nsv7019603copy number variation1nstd229human GRCh38 chr20: 31,763,891-31,974,358 , GRCh37.p13 chr20: 30,351,694-30,562,161 PDRG1, XKR7, 6 more genes
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6637514copy number variation1nstd102humanUncertain significance GRCh37 chr20: 30,299,729-30,687,587 , GRCh38.p12 chr20: 31,711,926-32,099,784 RNA5SP482, TTLL9, 13 more genes
    nsv6600035inversion1nstd223human GRCh38 chr20: 31,755,199-31,755,619 , GRCh37.p13 chr20: 30,343,002-30,343,422 TPX2
    nsv6597692inversion1nstd223human GRCh38 chr20: 31,743,469-31,743,900 , GRCh37.p13 chr20: 30,331,272-30,331,703 TPX2
    nsv6596699inversion1nstd223human GRCh38 chr20: 31,781,391-31,781,955 , GRCh37.p13 chr20: 30,369,194-30,369,758 TPX2
    nsv6534004copy number variation1nstd223human GRCh38 chr20: 31,750,646-31,751,839 , GRCh37.p13 chr20: 30,338,449-30,339,642 TPX2
    nsv6533691copy number variation1nstd223human GRCh38 chr20: 31,771,512-31,773,609 , GRCh37.p13 chr20: 30,359,315-30,361,412 TPX2
    nsv6527305copy number variation1nstd223human GRCh38 chr20: 31,763,891-31,974,354 , GRCh37.p13 chr20: 30,351,694-30,562,157 TTLL9, FOXS1, 6 more genes
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