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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5659896insertion1nstd207human GRCh38 chr15: 88,267,458-88,267,458 , GRCh37.p13 chr15: 88,810,689-88,810,689 NTRK3-AS1
    nsv5659097insertion1nstd207human GRCh38 chr15: 88,267,487-88,267,487 , GRCh37.p13 chr15: 88,810,718-88,810,718 NTRK3-AS1
    nsv5648397insertion1nstd207human GRCh38 chr15: 88,267,677-88,267,677 , GRCh37.p13 chr15: 88,810,908-88,810,908 NTRK3-AS1
    nsv5644639insertion1nstd207human GRCh38 chr15: 88,267,659-88,267,659 , GRCh37.p13 chr15: 88,810,890-88,810,890 NTRK3-AS1
    nsv5392905copy number variation1nstd186human GRCh37 chr15: 88,810,557-88,810,926 , GRCh38.p12 chr15: 88,267,326-88,267,695 NTRK3-AS1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5318623copy number variation1nstd204human GRCh38.p13 chr15: 88,266,878-88,268,108 , GRCh37.p13 chr15: 88,810,109-88,811,339 NTRK3-AS1
    nsv4863941copy number variation1nstd200human GRCh37 chr15: 88,810,500-88,810,965 , GRCh38.p12 chr15: 88,267,269-88,267,734 NTRK3-AS1
    nsv4756773insertion1nstd199human GRCh37 chr15: 88,810,803-88,810,803 , GRCh38.p12 chr15: 88,267,572-88,267,572 NTRK3-AS1
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4680817copy number variation1nstd189human GRCh38.p12 chr15: 88,231,494-88,435,522 , GRCh37.p13 chr15: 88,774,725-88,978,753 NTRK3, NTRK3-AS1, 3 more genes
    nsv4680722copy number variation1nstd189human GRCh38.p12 chr15: 88,258,540-88,435,522 , GRCh37.p13 chr15: 88,801,771-88,978,753 NTRK3-AS1, LOC105370957, 2 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
    nsv4250556copy number variation1nstd166human GRCh37.p13 chr15: 88,660,820-89,014,484 , GRCh38.p12 chr15: 88,117,589-88,471,253 NTRK3, MRPL46, 6 more genes
    nsv4245437copy number variation1nstd166human GRCh37.p13 chr15: 88,800,967-88,801,034 , GRCh38.p12 chr15: 88,257,736-88,257,803 NTRK3-AS1
    nsv3924544copy number variation1nstd102humanUncertain significance NCBI36 chr15: 86,443,734-86,819,080 , GRCh37.p13 chr15: 88,642,730-89,018,076 , GRCh38.p12 chr15: 88,099,499-88,474,845 MRPL46, MED28P6, 6 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3920352copy number variation1nstd102humanPathogenic GRCh38 chr15: 83,711,377-101,843,270 , NCBI36 chr15: 82,171,133-100,200,996 , GRCh37 chr15: 84,380,129-102,383,473 LOC102724465, SNRPA1, 333 more genes
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