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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938395copy number variation1nstd209human GRCh38 chr13: 37,105,475-37,108,490 , GRCh37.p13 chr13: 37,679,612-37,682,627 CSNK1A1L
    nsv5866930copy number variation1nstd209human GRCh38 chr13: 37,105,381-37,108,515 , GRCh37.p13 chr13: 37,679,518-37,682,652 CSNK1A1L
    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
    nsv5004456copy number variation1nstd200human GRCh38 chr13: 31,196,586-38,438,583 , GRCh37.p13 chr13: 31,770,723-39,012,720 , LOC102723490, 82 more genes
    nsv4997004copy number variation1nstd200human GRCh38 chr13: 37,105,475-37,108,491 , GRCh37.p13 chr13: 37,679,612-37,682,628 CSNK1A1L
    nsv4615396copy number variation2nstd183human GRCh37 chr13: 37,679,949-37,681,397 , GRCh38.p12 chr13: 37,105,812-37,107,260 CSNK1A1L
    nsv4530156copy number variation1nstd166human GRCh37.p13 chr13: 37,633,999-37,687,000 , GRCh38.p12 chr13: 37,059,862-37,112,863 CSNK1A1L, SUPT20H
    nsv4224991copy number variation1nstd166human GRCh37.p13 chr13: 37,267,644-37,768,435 , GRCh38.p12 chr13: 36,693,507-37,194,298 , RN7SKP1, 15 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
    nsv3924246copy number variation1nstd102humanPathogenic NCBI36 chr13: 29,785,946-38,739,818 , GRCh37 chr13: 30,887,946-39,841,818 , GRCh38 chr13: 30,313,809-39,267,681 LINC01048, N4BP2L2-IT2, 117 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
    nsv3917322copy number variation2nstd102humanPathogenic NCBI36 chr13: 19,309,535-114,110,750 , GRCh37 chr13: 20,411,535-115,085,141 , GRCh38 chr13: 19,837,395-114,327,173 RNY1P7, LINC01039, 1283 more genes
    nsv3917270copy number variation1nstd102humanPathogenic GRCh37 chr13: 33,105,623-87,409,299 , NCBI36 chr13: 32,003,623-86,207,300 , GRCh38 chr13: 32,531,486-86,757,044 LINC00366, PPIAP26, 663 more genes
    nsv3916629copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,139,188-115,085,141 , NCBI36 chr13: 18,037,188-114,110,750 , GRCh38 chr13: 18,565,048-114,327,173 TM9SF2, LOC107984564, 1330 more genes
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