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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975068inversion1nstd209human GRCh38 chr13: 24,966,165-25,349,536 , GRCh37.p13 chr13: 25,540,303-25,923,674 PABPC3, MTMR6, 12 more genes
    nsv5974508inversion1nstd209human GRCh38 chr13: 24,952,930-25,309,954 , GRCh37.p13 chr13: 25,527,068-25,884,092 PABPC3, MTMR6, 12 more genes
    nsv5935336copy number variation1nstd209human GRCh38 chr13: 25,318,972-25,319,081 , GRCh37.p13 chr13: 25,893,110-25,893,219 NUP58
    nsv5602134copy number variation1nstd207human GRCh38 chr13: 25,309,792-25,309,850 , GRCh37.p13 chr13: 25,883,930-25,883,988 NUP58
    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
    nsv5495410copy number variation1nstd206human GRCh38 chr13: 25,340,913-25,346,726 , GRCh37.p13 chr13: 25,915,051-25,920,864 NUP58
    nsv5342832translocation1nstd200human GRCh37 chr13: 25,894,958-25,894,958 , GRCh37 chr13: 25,895,024-25,895,024 , GRCh38.p12 chr13: 25,320,886-25,320,886 , GRCh38.p12 chr13: 25,320,820-25,320,820 NUP58
    nsv5158886mobile element insertion1nstd203human GRCh38 chr13: 25,304,235-25,304,251 , GRCh37.p13 chr13: 25,878,373-25,878,389 NUP58
    nsv4996636copy number variation1nstd200human GRCh38 chr13: 25,320,819-25,320,886 , GRCh37.p13 chr13: 25,894,957-25,895,024 NUP58
    nsv4729520copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 23,775,339-30,534,624 , GRCh38.p12 chr13: 23,201,200-29,960,487 PARP4, ATP12A, 136 more genes
    nsv4609670copy number variation1nstd183human GRCh37 chr13: 25,907,278-25,911,319 , GRCh38.p12 chr13: 25,333,140-25,337,181 NUP58
    nsv4599046copy number variation1nstd183human GRCh37 chr13: 25,910,483-25,911,242 , GRCh38.p12 chr13: 25,336,345-25,337,104 NUP58
    nsv4457197copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,069,228-27,474,401 , GRCh38.p12 chr13: 19,495,088-26,900,264 ZDHHC20, ANKRD20A10P, 154 more genes
    nsv4230498copy number variation1nstd166human GRCh37.p13 chr13: 25,881,978-25,983,333 , GRCh38.p12 chr13: 25,307,840-25,409,195 ELOBP1, NUP58, 1 more genes
    nsv4214037copy number variation1nstd166human GRCh37.p13 chr13: 25,895,142-25,895,472 , GRCh38.p12 chr13: 25,321,004-25,321,334 NUP58
    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
    nsv3923589copy number variation1nstd102humanUncertain significance NCBI36 chr13: 24,775,058-25,343,960 , GRCh37.p13 chr13: 25,877,058-26,445,960 , GRCh38.p12 chr13: 25,302,920-25,871,822 RNU6-78P, ATP8A2, 2 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
    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
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