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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7093895copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,428,449-89,725,229 , GRCh38.p12 chr10: 86,668,692-87,965,472 LOC105378410, PAPSS2, 33 more genes
    nsv7093742copy number variation1nstd102humanUncertain significance GRCh37 chr10: 89,621,946-89,623,527 , GRCh38.p12 chr10|NW_013171807.1: 78,013-79,594 , GRCh38.p12 chr10: 87,862,189-87,863,770 KLLN, PTEN
    nsv7093741copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,514,444-90,537,999 , GRCh38.p12 chr10: 87,754,687-88,778,242 LIPK, LOC105378416, 18 more genes
    nsv7093655copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,621,800-89,725,321 , GRCh38.p12 chr10: 87,862,043-87,965,564 , GRCh38.p12 chr10|NW_013171807.1: 77,867-181,353 KLLN, PTEN, 1 more genes
    nsv7093654copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,621,800-89,685,324 , GRCh38.p12 chr10|NW_013171807.1: 77,867-141,359 , GRCh38.p12 chr10: 87,862,043-87,925,567 KLLN, PTEN
    nsv7074617inversion1nstd229human GRCh38 chr10: 86,025,751-89,446,782 , GRCh37.p13 chr10: 87,785,508-91,206,539 GRID1, LDB3, 83 more genes
    nsv7073898inversion1nstd229human GRCh38 chr10: 85,457,267-89,078,986 , GRCh37.p13 chr10: 87,217,024-90,838,743 LOC112268064, LOC105378416, 74 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7070109inversion1nstd229human GRCh38 chr10: 87,536,871-87,971,064 , GRCh37.p13 chr10: 89,296,628-89,730,821 PAPSS2, PTEN, 8 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6894641copy number variation1nstd229human GRCh38 chr10: 87,858,669-87,860,016 , GRCh37.p13 chr10: 89,618,426-89,619,773 KLLN
    nsv6887185copy number variation1nstd229human GRCh38 chr10: 87,697,646-87,863,204 , GRCh37.p13 chr10: 89,457,403-89,622,961 KLLN, PTEN, 4 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6634664copy number variation1nstd102humanUncertain significance GRCh37 chr10: 89,622,972-89,623,860 , GRCh38 chr10: 87,863,215-87,864,103 KLLN, PTEN
    nsv6634648copy number variation1nstd102humanUncertain significance GRCh37 chr10: 89,623,248-89,623,354 , GRCh38 chr10: 87,863,491-87,863,597 PTEN, KLLN
    nsv6634458copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320 IFIT5, IFIT1, 140 more genes
    nsv6443208copy number variation1nstd223human GRCh38 chr10: 87,862,001-87,864,500 , GRCh37.p13 chr10: 89,621,758-89,624,257 KLLN, PTEN
    nsv6441239copy number variation1nstd223human GRCh38 chr10: 87,858,468-87,860,015 , GRCh37.p13 chr10: 89,618,225-89,619,772 KLLN
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