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Items: 1 to 20 of 153

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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
    nsv5503037copy number variation1nstd206human GRCh38 chr13: 36,671,688-36,672,699 , GRCh37.p13 chr13: 37,245,825-37,246,836 SERTM1, LOC102723490
    nsv5196543mobile element insertion1nstd203human GRCh38 chr13: 36,676,379-36,676,393 , GRCh37.p13 chr13: 37,250,516-37,250,530 SERTM1, LOC102723490
    nsv5004490copy number variation1nstd200human GRCh38 chr13: 36,672,217-36,672,927 , GRCh37.p13 chr13: 37,246,354-37,247,064 SERTM1, LOC102723490
    nsv5004489copy number variation1nstd200human GRCh38 chr13: 36,671,616-36,672,770 , GRCh37.p13 chr13: 37,245,753-37,246,907 LOC102723490, SERTM1
    nsv5004456copy number variation1nstd200human GRCh38 chr13: 31,196,586-38,438,583 , GRCh37.p13 chr13: 31,770,723-39,012,720 , LOC102723490, 82 more genes
    nsv4996989copy number variation1nstd200human GRCh38 chr13: 36,691,634-36,691,706 , GRCh37.p13 chr13: 37,265,771-37,265,843 LOC102723490, SERTM1
    nsv4672172copy number variation1nstd186human GRCh37 chr13: 37,245,837-37,246,851 , GRCh38.p12 chr13: 36,671,700-36,672,714 LOC102723490, SERTM1
    nsv4611462copy number variation1nstd183human GRCh37 chr13: 37,245,837-37,246,851 , GRCh38.p12 chr13: 36,671,700-36,672,714 SERTM1, LOC102723490
    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
    nsv4214328copy number variation1nstd166human GRCh37.p13 chr13: 37,246,401-37,247,025 , GRCh38.p12 chr13: 36,672,264-36,672,888 SERTM1, LOC102723490
    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
    nsv3922472copy number variation1nstd102humanPathogenic NCBI36 chr13: 28,793,591-36,467,485 , GRCh38 chr13: 29,321,454-36,995,348 , GRCh37 chr13: 29,895,591-37,569,485 LINC00445, CCDC169, 103 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
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