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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950011insertion1nstd209human GRCh38 chr9: 126,660,019-126,660,019 , GRCh37.p13 chr9: 129,422,298-129,422,298 LMX1B
    nsv5917270copy number variation1nstd209human GRCh38 chr9: 126,659,823-126,659,930 , GRCh37.p13 chr9: 129,422,102-129,422,209 LMX1B
    nsv5916640copy number variation1nstd209human GRCh38 chr9: 126,661,199-126,661,270 , GRCh37.p13 chr9: 129,423,478-129,423,549 LMX1B
    nsv5915738copy number variation1nstd209human GRCh38 chr9: 126,701,273-126,701,566 , GRCh37.p13 chr9: 129,463,552-129,463,845 LMX1B
    nsv5911947copy number variation1nstd209human GRCh38 chr9: 126,679,280-126,679,348 , GRCh37.p13 chr9: 129,441,559-129,441,627 LMX1B
    nsv5907703copy number variation1nstd209human GRCh38 chr9: 126,665,228-126,665,538 , GRCh37.p13 chr9: 129,427,507-129,427,817 LMX1B
    nsv5673880copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,376,729-129,377,858 , GRCh38.p12 chr9: 126,614,450-126,615,579 LMX1B
    nsv5629472insertion1nstd207human GRCh38 chr9: 126,660,172-126,660,172 , GRCh37.p13 chr9: 129,422,451-129,422,451 LMX1B
    nsv5626993insertion1nstd207human GRCh38 chr9: 126,660,019-126,660,019 , GRCh37.p13 chr9: 129,422,298-129,422,298 LMX1B
    nsv5624813insertion1nstd207human GRCh38 chr9: 126,701,273-126,701,273 , GRCh37.p13 chr9: 129,463,552-129,463,552 LMX1B
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 PIP5KL1, MIR3911, 50 more genes
    nsv5556707sequence alteration1nstd206human GRCh38 chr9: 126,660,074-126,660,074 , GRCh37.p13 chr9: 129,422,353-129,422,353 LMX1B
    nsv5491442copy number variation1nstd206human GRCh38 chr9: 126,663,127-126,664,673 , GRCh37.p13 chr9: 129,425,406-129,426,952 LMX1B
    nsv5491301copy number variation1nstd206human GRCh38 chr9: 126,701,273-126,701,570 , GRCh37.p13 chr9: 129,463,552-129,463,849 LMX1B
    nsv5483668copy number variation1nstd206human GRCh38 chr9: 126,631,516-126,632,691 , GRCh37.p13 chr9: 129,393,795-129,394,970 LMX1B
    nsv5386226copy number variation2nstd186human GRCh37 chr9: 129,422,291-129,422,595 , GRCh38.p12 chr9: 126,660,012-126,660,316 LMX1B
    nsv5379518translocation1nstd200human GRCh38 chr9: 126,680,923-126,680,923 , GRCh38 chr9: 126,680,495-126,680,495 , GRCh37.p13 chr9: 129,443,202-129,443,202 , GRCh37.p13 chr9: 129,442,774-129,442,774 LMX1B
    nsv5317515copy number variation1nstd204human GRCh38.p13 chr9: 126,631,493-126,632,712 , GRCh37.p13 chr9: 129,393,772-129,394,991 LMX1B
    nsv5311580copy number variation1nstd204human GRCh38.p13 chr9: 126,660,002-126,660,325 , GRCh37.p13 chr9: 129,422,281-129,422,604 LMX1B
    nsv5310646copy number variation1nstd204human GRCh38.p13 chr9: 126,701,249-126,701,585 , GRCh37.p13 chr9: 129,463,528-129,463,864 LMX1B
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