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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6871369copy number variation1nstd229human GRCh38 chr9: 124,004,801-124,370,400 , GRCh37.p13 chr9: 126,767,080-127,132,679 LHX2, PSMB7, 5 more genes
    nsv6865573copy number variation1nstd229human GRCh38 chr9: 124,027,124-124,029,829 , GRCh37.p13 chr9: 126,789,403-126,792,108 LHX2
    nsv6863092copy number variation1nstd229human GRCh38 chr9: 124,012,301-124,014,000 , GRCh37.p13 chr9: 126,774,580-126,776,279 LHX2
    nsv6861525copy number variation1nstd229human GRCh38 chr9: 124,032,858-124,037,058 , GRCh37.p13 chr9: 126,795,137-126,799,337 LOC107987037, LHX2
    nsv6637981copy number variation1nstd102humanPathogenic GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289 PBX3-DT, ADGRD2, 119 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6437604copy number variation1nstd223human GRCh38 chr9: 124,027,119-124,029,823 , GRCh37.p13 chr9: 126,789,398-126,792,102 LHX2
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291398copy number variation1nstd102humanPathogenic GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626 ZBTB6, LOC105376253, 107 more genes
    nsv6137443copy number variation1nstd213human GRCh37 chr9: 126,390,000-129,240,001 , GRCh38.p12 chr9: 123,627,721-126,477,722 NR6A1, GOLGA1, 52 more genes
    nsv6136365copy number variation1nstd213human GRCh37 chr9: 126,700,000-126,910,001 , GRCh38.p12 chr9: 123,937,721-124,147,722 LHX2, LHX2-AS1, 2 more genes
    nsv5854928copy number variation2nstd209human GRCh38 chr9: 124,010,719-124,012,366 , GRCh37.p13 chr9: 126,772,998-126,774,645 LHX2
    nsv5120799mobile element insertion1nstd203human GRCh38 chr9: 124,028,042-124,028,057 , GRCh37.p13 chr9: 126,790,321-126,790,336 LHX2
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4492335mobile element insertion1nstd166human GRCh37.p13 chr9: 126,790,318-126,790,318 , GRCh38.p12 chr9: 124,028,039-124,028,039 LHX2
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
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