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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv6932013copy number variation1nstd229human GRCh38 chr13: 27,894,801-28,169,500 , GRCh37.p13 chr13: 28,468,938-28,743,637 URAD, CDX2, 12 more genes
    nsv6925353copy number variation1nstd229human GRCh38 chr13: 27,959,539-27,959,732 , GRCh37.p13 chr13: 28,533,676-28,533,869 CDX2
    nsv6923867copy number variation1nstd229human GRCh38 chr13: 27,967,680-27,967,800 , GRCh37.p13 chr13: 28,541,817-28,541,937 CDX2
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6132752copy number variation1nstd213human GRCh37 chr13: 27,480,000-28,970,001 , GRCh38.p12 chr13: 26,905,863-28,395,864 CDX2, FLT1, 41 more genes
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6132475copy number variation1nstd213human GRCh37 chr13: 26,620,000-32,650,001 , GRCh38.p12 chr13: 26,045,862-32,075,864 ALOX5AP, HMGB1, 106 more genes
    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
    nsv5362404translocation1nstd200human GRCh38 chr13: 27,967,175-27,967,175 , GRCh38 chr5: 90,155,662-90,155,662 , GRCh37.p13 chr13: 28,541,312-28,541,312 , GRCh37.p13 chr5: 89,451,479-89,451,479 CDX2
    nsv5340050translocation1nstd200human GRCh37 chr5: 89,451,479-89,451,479 , GRCh37 chr13: 28,541,312-28,541,312 , GRCh38.p12 chr5: 90,155,662-90,155,662 , GRCh38.p12 chr13: 27,967,175-27,967,175 CDX2
    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
    nsv4675905copy number variation1nstd102humanUncertain significance GRCh37 chr13: 28,083,408-28,591,050 , GRCh38.p12 chr13: 27,509,271-28,016,913 PDX1, PLUT, 14 more genes
    nsv4600390copy number variation1nstd183human GRCh37 chr13: 28,496,771-28,541,762 , GRCh38.p12 chr13: 27,922,634-27,967,625 ATP5F1EP2, LINC00543, 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
    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
    nsv3921601copy number variation1nstd102humanLikely pathogenic NCBI36 chr13: 26,437,381-29,569,995 , GRCh37 chr13: 27,539,381-30,671,995 , GRCh38 chr13: 26,965,244-30,097,858 CDX2, FLT1, 58 more genes
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