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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5848201copy number variation1nstd209human GRCh38 chr13: 27,872,536-27,877,270 , GRCh37.p13 chr13: 28,446,673-28,451,407 PLUT
    nsv5649664insertion1nstd207human GRCh38 chr13: 27,839,538-27,839,538 , GRCh37.p13 chr13: 28,413,675-28,413,675 PLUT
    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
    nsv5268252copy number variation1nstd204human GRCh38.p13 chr13: 27,891,001-27,893,800 , GRCh37.p13 chr13: 28,465,138-28,467,937 PLUT
    nsv5151114mobile element insertion1nstd203human GRCh38 chr13: 27,844,608-27,844,621 , GRCh37.p13 chr13: 28,418,745-28,418,758 PLUT
    nsv5004436copy number variation1nstd200human GRCh38 chr13: 27,831,474-27,862,176 , GRCh37.p13 chr13: 28,405,611-28,436,313 PLUT
    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
    nsv4529286copy number variation1nstd166human GRCh37.p13 chr13: 28,446,285-28,446,964 , GRCh38.p12 chr13: 27,872,148-27,872,827 PLUT
    nsv4512962mobile element insertion1nstd166human GRCh37.p13 chr13: 28,451,510-28,451,510 , GRCh38.p12 chr13: 27,877,373-27,877,373 PLUT
    nsv4512351mobile element insertion1nstd166human GRCh37.p13 chr13: 28,453,049-28,453,049 , GRCh38.p12 chr13: 27,878,912-27,878,912 PLUT
    nsv4503822mobile element insertion1nstd166human GRCh37.p13 chr13: 28,441,509-28,441,509 , GRCh38.p12 chr13: 27,867,372-27,867,372 PLUT
    nsv4390562copy number variation1nstd171human GRCh37 chr13: 28,450,489-28,450,523 , GRCh38.p12 chr13: 27,876,352-27,876,386 PLUT
    nsv4375885copy number variation1nstd173human GRCh37 chr13: 28,486,188-28,522,031 , GRCh38.p12 chr13: 27,912,051-27,947,894 PLUT, ATP5F1EP2, 1 more genes
    nsv4308033insertion1nstd166human GRCh37.p13 chr13: 28,473,271-28,473,271 , GRCh38.p12 chr13: 27,899,134-27,899,134 PLUT
    nsv4230182copy number variation1nstd166human GRCh37.p13 chr13: 28,417,586-28,418,370 , GRCh38.p12 chr13: 27,843,449-27,844,233 PLUT
    nsv4218500copy number variation1nstd166human GRCh37.p13 chr13: 28,458,761-28,461,164 , GRCh38.p12 chr13: 27,884,624-27,887,027 PLUT
    nsv3968259insertion1nstd168human GRCh38 chr13: 27,909,039-27,922,467 , GRCh37.p13 chr13: 28,483,176-28,496,604 PLUT, PDX1
    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
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