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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5500100copy number variation1nstd206human GRCh38 chr13: 41,132,000-41,193,553 , GRCh37.p13 chr13: 41,706,136-41,767,689 KBTBD6, CALM2P3, 2 more genes
    nsv5004516copy number variation1nstd200human GRCh38 chr13: 41,131,628-41,193,655 , GRCh37.p13 chr13: 41,705,764-41,767,791 CALM2P3, KBTBD7, 2 more genes
    nsv5004515copy number variation1nstd200human GRCh38 chr13: 41,125,513-41,126,046 , GRCh37.p13 chr13: 41,699,649-41,700,182 KBTBD6
    nsv4842498copy number variation1nstd200human GRCh37 chr13: 41,699,649-41,700,182 , GRCh38.p12 chr13: 41,125,513-41,126,046 KBTBD6
    nsv4675893copy number variation1nstd102humanUncertain significance GRCh37 chr13: 41,703,612-41,769,277 , GRCh38.p12 chr13: 41,129,476-41,195,141 CALM2P3, KBTBD6, 2 more genes
    nsv4675658copy number variation1nstd102humanUncertain significance GRCh37 chr13: 41,383,468-41,902,324 , GRCh38.p12 chr13: 40,809,332-41,328,188 KBTBD6, WBP4, 18 more genes
    nsv4602264copy number variation1nstd183human GRCh37 chr13: 40,306,065-46,460,742 , GRCh38.p12 chr13: 39,731,928-45,886,607 , RN7SKP2, 127 more genes
    nsv4529224copy number variation1nstd166human GRCh37.p13 chr13: 41,705,999-41,767,500 , GRCh38.p12 chr13: 41,131,863-41,193,364 CALM2P3, KBTBD6-DT, 2 more genes
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3923911copy number variation1nstd102humanPathogenic GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921 MLNR, SIAH3, 422 more genes
    nsv3923636copy number variation1nstd102humanPathogenic NCBI36 chr13: 37,986,314-50,897,351 , GRCh37 chr13: 39,088,314-51,999,350 , GRCh38 chr13: 38,514,177-51,425,214 TUSC8, SNORA31B, 251 more genes
    nsv3922463copy number variation1nstd102humanPathogenic NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628 TULP3P1, LOC105370349, 1311 more genes
    nsv3921404copy number variation1nstd102humanPathogenic GRCh37 chr13: 31,592,297-49,065,340 , GRCh38 chr13: 31,018,160-48,491,204 , NCBI36 chr13: 30,490,297-47,963,341 MIR8079, ZDHHC4P1, 280 more genes
    nsv3921223copy number variation1nstd102humanPathogenic GRCh38 chr13: 19,671,934-114,340,331 , NCBI36 chr13: 19,144,074-114,123,908 , GRCh37 chr13: 20,246,074-115,085,141 TRIM60P13, LINC00351, 1289 more genes
    nsv3920749copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,407,270-115,064,089 , GRCh38 chr13: 19,833,130-114,298,614 , NCBI36 chr13: 19,305,270-114,082,191 DIAPH3-AS2, LOC105370216, 1281 more genes
    nsv3920039copy number variation2nstd102humanPathogenic GRCh37 chr13: 31,937,609-91,227,546 , NCBI36 chr13: 30,835,609-90,025,547 , GRCh38 chr13: 31,363,472-90,575,292 PSMD10P3, CPB2, 714 more genes
    nsv3919574copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,850,545-114,327,173 , GRCh37 chr13: 19,296,527-115,085,141 , NCBI36 chr13: 18,194,527-114,110,750 RNU6-77P, LINC00457, 1317 more genes
    nsv3919427copy number variation1nstd102humanPathogenic NCBI36 chr13: 31,025,745-64,942,500 , GRCh37 chr13: 32,127,745-66,044,499 , GRCh38 chr13: 31,553,608-65,470,367 PCDH8, TRIM13, 469 more genes
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