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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148086copy number variation1nstd102humanPathogenic GRCh37 chr10: 124,895,517-135,440,296 , GRCh38.p12 chr10: 123,136,001-133,626,792 FANK1, LOC105378534, 159 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7137208copy number variation1nstd102humanPathogenic GRCh37 chr10: 123,477,898-135,427,143 , GRCh38.p12 chr10: 121,718,384-133,613,639 ZRANB1, LOC105378544, 182 more genes
    nsv7098893copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306 LOC105378571, DOCK1, 196 more genes
    nsv7068454inversion1nstd229human GRCh38 chr10: 124,712,997-124,715,876 , GRCh37.p13 chr10: 126,401,566-126,404,445 FAM53B-AS1, FAM53B
    nsv7068192inversion1nstd229human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 CTBP2, RPS26P39, 114 more genes
    nsv6897984copy number variation1nstd229human GRCh38 chr10: 124,702,783-124,705,717 , GRCh37.p13 chr10: 126,391,352-126,394,286 FAM53B-AS1, FAM53B
    nsv6887005copy number variation1nstd229human GRCh38 chr10: 124,587,801-124,741,400 , GRCh37.p13 chr10: 126,276,370-126,429,969 FAM53B-AS1, LHPP, 1 more genes
    nsv6885368copy number variation1nstd229human GRCh38 chr10: 124,388,001-124,753,400 , GRCh37.p13 chr10: 126,076,570-126,441,969 OATP1, OAT, 5 more genes
    nsv6885102copy number variation1nstd229human GRCh38 chr10: 124,141,254-125,049,887 , GRCh37.p13 chr10: 125,919,474-126,738,456 OATP1, LHPP, 13 more genes
    nsv6884703copy number variation1nstd229human GRCh38 chr10: 121,934,615-128,427,106 , GRCh37.p13 chr10: 123,694,130-130,225,370 OAT, C10orf88, 98 more genes
    nsv6881912copy number variation1nstd229human GRCh38 chr10: 124,677,096-124,832,734 , GRCh37.p13 chr10: 126,365,665-126,521,303 FAM53B-AS1, EEF1AKMT2, 2 more genes
    nsv6585886inversion1nstd223human GRCh38 chr10: 118,910,158-125,783,778 , GRCh37.p13 chr10: 120,669,670-127,472,347 LOC105378520, SPADH, 114 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6313907copy number variation1nstd102humanUncertain significance GRCh37 chr10: 125,920,216-126,732,932 , GRCh38.p12 chr10: 124,231,647-125,044,363 CTBP2, MIR4296, 12 more genes
    nsv6131941copy number variation1nstd213human GRCh37 chr10: 126,350,000-126,470,001 , GRCh38.p12 chr10: 124,661,431-124,781,432 FAM53B, EEF1AKMT2, 1 more genes
    nsv6131940copy number variation2nstd213human GRCh37 chr10: 125,920,000-128,610,001 , GRCh38.p12 chr10: 124,231,431-126,921,432 ALDOAP2, CTBP2, 47 more genes
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
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