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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5932585copy number variation1nstd209human GRCh38 chr14: 52,665,709-52,665,769 , GRCh37.p13 chr14: 53,132,427-53,132,487 ERO1A
    nsv5728600mobile element insertion1nstd211human GRCh38 chr14: 52,637,967-52,637,967 , GRCh37.p13 chr14: 53,104,685-53,104,685 GPR137C, ERO1A
    nsv5712161mobile element insertion1nstd211human GRCh38 chr14: 52,652,026-52,652,026 , GRCh37.p13 chr14: 53,118,744-53,118,744 ERO1A
    nsv5548918insertion1nstd206human GRCh38 chr14: 52,637,967-52,638,004 , GRCh37.p13 chr14: 53,104,685-53,104,722 GPR137C, ERO1A
    nsv5332041translocation1nstd200human GRCh37 chr9: 136,896,291-136,896,291 , GRCh37 chr14: 53,142,158-53,142,158 , GRCh38.p12 chr14: 52,675,440-52,675,440 , GRCh38.p12 chr9: 134,031,169-134,031,169 BRD3, ERO1A, 1 more genes
    nsv5183641mobile element insertion1nstd203human GRCh38 chr14: 52,653,551-52,653,564 , GRCh37.p13 chr14: 53,120,269-53,120,282 ERO1A
    nsv4999397copy number variation1nstd200human GRCh38 chr14: 52,684,027-52,684,189 , GRCh37.p13 chr14: 53,150,745-53,150,907 ERO1A
    nsv4999396copy number variation1nstd200human GRCh38 chr14: 52,649,780-52,655,017 , GRCh37.p13 chr14: 53,116,498-53,121,735 ERO1A
    nsv4843727copy number variation1nstd200human GRCh37 chr14: 53,116,498-53,121,735 , GRCh38.p12 chr14: 52,649,780-52,655,017 ERO1A
    nsv4833019copy number variation1nstd200human GRCh37 chr14: 53,143,400-53,143,938 , GRCh38.p12 chr14: 52,676,682-52,677,220 ERO1A
    nsv4830028copy number variation1nstd200human GRCh37 chr14: 53,139,809-53,139,862 , GRCh38.p12 chr14: 52,673,091-52,673,144 ERO1A
    nsv4728122copy number variation1nstd197human GRCh38.p12 chr14: 52,657,918-52,661,304 , GRCh37 chr14: 53,124,636-53,128,022 ERO1A
    nsv4619399copy number variation1nstd183human GRCh37 chr14: 53,138,428-53,138,641 , GRCh38.p12 chr14: 52,671,710-52,671,923 ERO1A
    nsv4577113mobile element insertion1nstd166human GRCh37.p13 chr14: 53,120,269-53,120,269 , GRCh38.p12 chr14: 52,653,551-52,653,551 ERO1A
    nsv4576696mobile element insertion1nstd166human GRCh37.p13 chr14: 53,128,048-53,128,048 , GRCh38.p12 chr14: 52,661,330-52,661,330 ERO1A
    nsv4555656insertion1nstd166human GRCh37.p13 chr14: 53,150,016-53,150,016 , GRCh38.p12 chr14: 52,683,298-52,683,298 ERO1A
    nsv4555421insertion1nstd166human GRCh37.p13 chr14: 53,154,605-53,154,605 , GRCh38.p12 chr14: 52,687,887-52,687,887 ERO1A
    nsv4505483mobile element insertion1nstd166human GRCh37.p13 chr14: 53,118,730-53,118,730 , GRCh38.p12 chr14: 52,652,012-52,652,012 ERO1A
    nsv4503178mobile element insertion1nstd166human GRCh37.p13 chr14: 53,113,206-53,113,206 , GRCh38.p12 chr14: 52,646,488-52,646,488 ERO1A
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