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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921253copy number variation1nstd209human GRCh38 chr9: 97,911,064-97,911,776 , GRCh37.p13 chr9: 100,673,346-100,674,058 TRMO
    nsv5916791copy number variation1nstd209human GRCh38 chr9: 97,896,725-97,896,908 , GRCh37.p13 chr9: 100,659,007-100,659,190 , TRMO
    nsv5854436copy number variation1nstd209human GRCh38 chr9: 97,900,311-97,901,310 , GRCh37.p13 chr9: 100,662,593-100,663,592 TRMO
    nsv5730760mobile element insertion2nstd211human GRCh38 chr9: 97,913,268-97,913,268 , GRCh37.p13 chr9: 100,675,550-100,675,550 TRMO
    nsv5713428mobile element insertion2nstd211human GRCh38 chr9: 97,895,580-97,895,580 , GRCh37.p13 chr9: 100,657,862-100,657,862 , TRMO
    nsv5626459insertion1nstd207human GRCh38 chr9: 97,913,251-97,913,251 , GRCh37.p13 chr9: 100,675,533-100,675,533 TRMO
    nsv5558541mobile element insertion1nstd206human GRCh38 chr9: 97,913,251-97,913,251 , GRCh37.p13 chr9: 100,675,533-100,675,533 TRMO
    nsv5489950copy number variation1nstd206human GRCh38 chr9: 97,896,725-97,896,911 , GRCh37.p13 chr9: 100,659,007-100,659,193 , TRMO
    nsv5478124copy number variation1nstd206human GRCh38 chr9: 97,911,064-97,911,778 , GRCh37.p13 chr9: 100,673,346-100,674,060 TRMO
    nsv5399769mobile element insertion1nstd206human GRCh38 chr9: 97,895,580-97,895,631 , GRCh37.p13 chr9: 100,657,862-100,657,913 , TRMO
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5353529translocation1nstd200human GRCh38 chr1: 85,933,338-85,933,338 , GRCh38 chr9: 97,913,267-97,913,267 , GRCh37.p13 chr9: 100,675,549-100,675,549 , GRCh37.p13 chr1: 86,399,021-86,399,021 TRMO, COL24A1
    nsv5199716mobile element insertion1nstd203human GRCh38 chr9: 97,913,256-97,913,268 , GRCh37.p13 chr9: 100,675,538-100,675,550 TRMO
    nsv5197891mobile element insertion1nstd203human GRCh38 chr9: 97,913,250-97,913,268 , GRCh37.p13 chr9: 100,675,532-100,675,550 TRMO
    nsv5193576mobile element insertion1nstd203human GRCh38 chr9: 97,913,255-97,913,268 , GRCh37.p13 chr9: 100,675,537-100,675,550 TRMO
    nsv5187407mobile element insertion1nstd203human GRCh38 chr9: 97,913,249-97,913,268 , GRCh37.p13 chr9: 100,675,531-100,675,550 TRMO
    nsv5185334mobile element insertion1nstd203human GRCh38 chr9: 97,913,258-97,913,268 , GRCh37.p13 chr9: 100,675,540-100,675,550 TRMO
    nsv5184926mobile element insertion1nstd203human GRCh38 chr9: 97,913,257-97,913,268 , GRCh37.p13 chr9: 100,675,539-100,675,550 TRMO
    nsv5180984mobile element insertion1nstd203human GRCh38 chr9: 97,913,251-97,913,268 , GRCh37.p13 chr9: 100,675,533-100,675,550 TRMO
    nsv5139060mobile element insertion1nstd203human GRCh38 chr9: 97,907,060-97,907,081 , GRCh37.p13 chr9: 100,669,342-100,669,363 TRMO
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