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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898458copy number variation1nstd209human GRCh38 chr3: 150,310,631-150,310,747 , GRCh37.p13 chr3: 150,028,418-150,028,534 LOC107986141, LINC01214
    nsv5693815mobile element insertion1nstd211human GRCh38 chr3: 150,319,630-150,319,630 , GRCh37.p13 chr3: 150,037,417-150,037,417 LINC01214, LOC107986141
    nsv5680796mobile element insertion1nstd211human GRCh38 chr3: 150,294,845-150,294,845 , GRCh37.p13 chr3: 150,012,632-150,012,632 LINC01214
    nsv5544724insertion1nstd206human GRCh38 chr3: 150,268,640-150,268,640 , GRCh37.p13 chr3: 149,986,427-149,986,427 LINC01214
    nsv5452755copy number variation1nstd206human GRCh38 chr3: 150,310,636-150,310,748 , GRCh37.p13 chr3: 150,028,423-150,028,535 LINC01214, LOC107986141
    nsv5396805mobile element insertion1nstd206human GRCh38 chr3: 150,319,630-150,319,681 , GRCh37.p13 chr3: 150,037,417-150,037,468 LINC01214, LOC107986141
    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
    nsv5338290translocation1nstd200human GRCh37 chr19: 24,342,111-24,342,111 , GRCh37 chr3: 149,986,450-149,986,450 , GRCh38.p12 chr3: 150,268,663-150,268,663 , GRCh38.p12 chr19: 24,159,309-24,159,309 LINC01214
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4912350copy number variation1nstd200human GRCh38 chr3: 150,269,529-150,270,402 , GRCh37.p13 chr3: 149,987,316-149,988,189 LINC01214
    nsv4912349copy number variation1nstd200human GRCh38 chr3: 150,262,013-150,270,960 , GRCh37.p13 chr3: 149,979,800-149,988,747 LINC01214
    nsv4797975copy number variation1nstd200human GRCh37 chr3: 149,979,800-149,988,747 , GRCh38.p12 chr3: 150,262,013-150,270,960 LINC01214
    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
    nsv4674717copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 144,053,029-150,272,658 , GRCh38.p12 chr3: 144,334,187-150,554,871 AGTR1, CP, 83 more genes
    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
    nsv4469433mobile element insertion1nstd166human GRCh37.p13 chr3: 149,995,392-149,995,392 , GRCh38.p12 chr3: 150,277,605-150,277,605 LINC01214, LOC105374154
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv4106817copy number variation1nstd166human GRCh37.p13 chr3: 150,028,423-150,028,535 , GRCh38.p12 chr3: 150,310,636-150,310,748 LINC01214, LOC107986141
    nsv4099521copy number variation1nstd166human GRCh37.p13 chr3: 149,987,316-149,988,189 , GRCh38.p12 chr3: 150,269,529-150,270,402 LINC01214
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