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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905651copy number variation1nstd209human GRCh38 chr3: 150,916,205-150,925,071 , GRCh37.p13 chr3: 150,633,992-150,642,858 CLRN1
    nsv5834367copy number variation1nstd209human GRCh38 chr3: 150,916,249-150,925,239 , GRCh37.p13 chr3: 150,634,036-150,643,026 CLRN1
    nsv5453185copy number variation1nstd206human GRCh38 chr3: 150,939,724-150,939,800 , GRCh37.p13 chr3: 150,657,511-150,657,587 CLRN1
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4924701copy number variation1nstd200human GRCh38 chr3: 150,944,054-150,958,116 , GRCh37.p13 chr3: 150,661,841-150,675,903 CLRN1
    nsv4912375copy number variation1nstd200human GRCh38 chr3: 150,941,313-150,946,988 , GRCh37.p13 chr3: 150,659,100-150,664,775 CLRN1
    nsv4912374copy number variation1nstd200human GRCh38 chr3: 150,936,541-150,938,146 , GRCh37.p13 chr3: 150,654,328-150,655,933 CLRN1
    nsv4875946mobile element deletion1nstd200human GRCh38 chr3: 150,948,202-150,948,508 , GRCh37.p13 chr3: 150,665,989-150,666,295 CLRN1
    nsv4804892copy number variation1nstd200human GRCh37 chr3: 150,661,841-150,675,903 , GRCh38.p12 chr3: 150,944,054-150,958,116 CLRN1
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4682168copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 150,658,258-150,663,476 , GRCh38.p12 chr3: 150,940,471-150,945,689 CLRN1
    nsv4674301copy number variation1nstd102humanPathogenic GRCh37 chr3: 149,404,255-152,786,331 , GRCh38.p12 chr3: 149,686,468-153,068,542 EIF3JP2, IGSF10, 63 more genes
    nsv4673991copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,534,295-151,213,925 , GRCh38.p12 chr3: 150,816,508-151,496,137 P2RY14, RNA5SP145, 11 more genes
    nsv4570893sequence alteration1nstd166human GRCh37.p13 chr3: 150,650,064-150,650,700 , GRCh38.p12 chr3: 150,932,277-150,932,913 CLRN1
    nsv4469440mobile element insertion1nstd166human GRCh37.p13 chr3: 150,681,711-150,681,711 , GRCh38.p12 chr3: 150,963,924-150,963,924 CLRN1
    nsv4469165mobile element insertion1nstd166human GRCh37.p13 chr3: 150,662,711-150,662,711 , GRCh38.p12 chr3: 150,944,924-150,944,924 CLRN1
    nsv4454990copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,647,395-150,665,244 , GRCh38.p12 chr3: 150,929,608-150,947,457 CLRN1
    nsv4454602copy number variation1nstd102humanPathogenic GRCh37 chr3: 150,690,233-150,690,796 , GRCh38 chr3: 150,972,446-150,973,009 CLRN1, CLRN1-AS1
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
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