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Items: 1 to 20 of 475

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070730inversion1nstd229human GRCh38 chr9: 62,058,130-67,204,238 , GRCh37.p13 chr9: 41,204,320-44,676,072 ATP5F1AP10, IGKV1OR9-1, 125 more genes
    nsv7066246inversion1nstd229human GRCh38 chr9: 61,567,441-63,740,704 , GRCh37.p13 chr: NaN-NaN FGF7P6, LOC105379807, 47 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
    nsv6455213copy number variation1nstd223human GRCh38 chr9: 63,360,401-63,370,300 , GRCh37.p13 chr9: 67,315,373-67,325,272 LOC100996643
    nsv6454968copy number variation1nstd223human GRCh38 chr9: 63,332,701-63,339,700 , GRCh37.p13 chr9: 67,287,673-67,294,672 AQP7P1, LOC100996643
    nsv6454754copy number variation1nstd223human GRCh38 chr9: 63,296,301-63,394,600 , GRCh37.p13 chr9: 67,251,273-67,349,572 AQP7P1, LOC100996643, 1 more genes
    nsv6454722copy number variation1nstd223human GRCh38 chr9: 63,350,701-63,355,200 , GRCh37.p13 chr9: 67,305,673-67,310,172 LOC100996643
    nsv6453762copy number variation1nstd223human GRCh38 chr9: 63,253,001-63,363,700 , GRCh37.p13 chr9: 67,207,973-67,318,672 AQP7P1, LOC100996643
    nsv6451988copy number variation1nstd223human GRCh38 chr9: 63,335,201-63,336,200 , GRCh37.p13 chr9: 67,290,173-67,291,172 LOC100996643
    nsv6450703copy number variation1nstd223human GRCh38 chr9: 63,314,301-63,336,000 , GRCh37.p13 chr9: 67,269,273-67,290,972 LOC100996643, AQP7P1
    nsv6450516copy number variation1nstd223human GRCh38 chr9: 63,351,101-63,359,000 , GRCh37.p13 chr9: 67,306,073-67,313,972 LOC100996643
    nsv6450298copy number variation1nstd223human GRCh38 chr9: 63,332,401-63,370,400 , GRCh37.p13 chr9: 67,287,373-67,325,372 AQP7P1, LOC100996643
    nsv6448825copy number variation1nstd223human GRCh38 chr9: 63,313,001-63,365,100 , GRCh37.p13 chr9: 67,267,973-67,320,072 LOC100996643, AQP7P1
    nsv6446135copy number variation1nstd223human GRCh38 chr9: 63,314,301-63,365,900 , GRCh37.p13 chr9: 67,269,273-67,320,872 LOC100996643, AQP7P1
    nsv6446044copy number variation1nstd223human GRCh38 chr9: 63,361,901-63,365,100 , GRCh37.p13 chr9: 67,316,873-67,320,072 LOC100996643
    nsv6446030copy number variation1nstd223human GRCh38 chr9: 63,349,601-63,394,700 , GRCh37.p13 chr9: 67,304,573-67,349,672 LOC100996643, BMS1P10
    nsv6445651copy number variation1nstd223human GRCh38 chr9: 63,340,901-63,415,100 , GRCh37.p13 chr9: 67,295,873-67,366,296 LOC105379442, BMS1P10, 1 more genes
    nsv6445493copy number variation1nstd223human GRCh38 chr9: 63,313,501-63,391,900 , GRCh37.p13 chr9: 67,268,473-67,346,872 BMS1P10, AQP7P1, 1 more genes
    nsv6443719copy number variation1nstd223human GRCh38 chr9: 63,349,501-63,354,600 , GRCh37.p13 chr9: 67,304,473-67,309,572 LOC100996643
    nsv6443173copy number variation1nstd223human GRCh38 chr9: 63,291,201-63,373,600 , GRCh37.p13 chr9: 67,246,173-67,328,572 AQP7P1, LOC100996643, 1 more genes
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