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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5695096mobile element insertion1nstd211human GRCh38 chr15: 83,111,558-83,111,558 , GRCh37.p13 chr15: 83,780,310-83,780,310 HDGFL3, TM6SF1
    nsv5522247copy number variation1nstd206human GRCh38 chr15: 83,119,383-83,119,536 , GRCh37.p13 chr15: 83,788,135-83,788,288 HDGFL3, TM6SF1
    nsv5520650copy number variation1nstd206human GRCh38 chr15: 83,108,449-83,108,543 , GRCh37.p13 chr15: 83,777,201-83,777,295 TM6SF1
    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
    nsv5153335mobile element insertion1nstd203human GRCh38 chr15: 83,140,984-83,140,999 , GRCh37.p13 chr15: 83,809,736-83,809,751 HDGFL3, TM6SF1
    nsv5142193mobile element insertion1nstd203human GRCh38 chr15: 83,111,543-83,111,555 , GRCh37.p13 chr15: 83,780,295-83,780,307 HDGFL3, TM6SF1
    nsv5002060copy number variation1nstd200human GRCh38 chr15: 83,124,184-83,124,272 , GRCh37.p13 chr15: 83,792,936-83,793,024 TM6SF1, HDGFL3
    nsv5002059copy number variation1nstd200human GRCh38 chr15: 83,123,429-83,131,054 , GRCh37.p13 chr15: 83,792,181-83,799,806 HDGFL3, TM6SF1
    nsv5002058copy number variation1nstd200human GRCh38 chr15: 83,115,191-83,121,122 , GRCh37.p13 chr15: 83,783,943-83,789,874 TM6SF1, HDGFL3
    nsv4856097copy number variation1nstd200human GRCh37 chr15: 83,783,943-83,789,875 , GRCh38.p12 chr15: 83,115,191-83,121,123 TM6SF1, HDGFL3
    nsv4729284copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,201,955-85,786,847 , GRCh38.p12 chr15: 82,641,775-85,243,616 GOLGA6L5P, DNM1P44, 77 more genes
    nsv4578262copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,214,012-84,772,030 , GRCh38.p12 chr15: 82,641,775-84,103,278 LOC100421235, LOC105370933, 29 more genes
    nsv4513475mobile element insertion1nstd166human GRCh37.p13 chr15: 83,780,295-83,780,295 , GRCh38.p12 chr15: 83,111,543-83,111,543 HDGFL3, TM6SF1
    nsv4456897copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,468,371-84,797,068 , GRCh38.p12 chr15: 82,176,030-84,128,316 HDGFL3, LOC105370926, 46 more genes
    nsv4456639copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,728,654-84,107,646 , GRCh38.p12 chr15: 80,436,313-83,438,894 LOC100288241, LOC105370926, 64 more genes
    nsv4455892copy number variation1nstd102humanPathogenic GRCh37 chr15: 82,688,216-84,796,779 , GRCh38.p12 chr15: 82,396,005-84,128,027 UBE2Q2P2, GOLGA2P10, 40 more genes
    nsv4416976copy number variation1nstd174human GRCh37 chr15: 83,773,683-83,774,400 , GRCh38.p12 chr15: 83,104,931-83,105,648 TM6SF1
    nsv4248501copy number variation1nstd166human GRCh37.p13 chr15: 83,810,061-83,810,181 , GRCh38.p12 chr15: 83,141,309-83,141,429 TM6SF1, HDGFL3
    nsv4245691copy number variation1nstd166human GRCh37.p13 chr15: 83,809,669-83,812,903 , GRCh38.p12 chr15: 83,140,917-83,144,151 HDGFL3, TM6SF1
    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
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