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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6873976copy number variation1nstd229human GRCh38 chr9: 116,805,522-117,273,359 , GRCh37.p13 chr9: 119,567,801-120,035,638 ASTN2, RN7SKP128, 5 more genes
    nsv6872378copy number variation1nstd229human GRCh38 chr9: 116,987,526-119,256,739 , GRCh37.p13 chr9: 119,749,805-122,019,017 LOC101928849, LOC105376249, 21 more genes
    nsv6870527copy number variation1nstd229human GRCh38 chr9: 117,143,913-117,190,317 , GRCh37.p13 chr9: 119,906,192-119,952,596 ASTN2, RPL10P3, 1 more genes
    nsv6868842copy number variation1nstd229human GRCh38 chr9: 117,170,788-117,189,134 , GRCh37.p13 chr9: 119,933,067-119,951,413 SNORA70C, ASTN2, 1 more genes
    nsv6868431copy number variation1nstd229human GRCh38 chr9: 117,138,223-117,195,461 , GRCh37.p13 chr9: 119,900,502-119,957,740 SNORA70C, ASTN2, 3 more genes
    nsv6863356copy number variation1nstd229human GRCh38 chr9: 116,864,051-117,246,873 , GRCh37.p13 chr9: 119,626,330-120,009,152 SNORA70C, ASTN2, 3 more genes
    nsv6858185copy number variation1nstd229human GRCh38 chr9: 117,122,195-117,231,372 , GRCh37.p13 chr9: 119,884,474-119,993,651 RPL10P3, ASTN2, 3 more genes
    nsv6637920copy number variation1nstd102humanUncertain significance GRCh37 chr9: 119,459,011-120,434,018 , GRCh38.p12 chr9: 116,696,732-117,671,740 RN7SKP125, RPL10P3, 9 more genes
    nsv6637476copy number variation1nstd102humanUncertain significance GRCh37 chr9: 119,836,696-119,958,853 , GRCh38.p12 chr9: 117,074,417-117,196,574 RN7SKP128, LOC105376237, 3 more genes
    nsv6637448copy number variation1nstd102humanUncertain significance GRCh37 chr9: 119,759,114-120,060,374 , GRCh38.p12 chr9: 116,996,835-117,298,095 SNORA70C, RN7SKP125, 4 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
    nsv6436890copy number variation1nstd223human GRCh38 chr9: 117,122,195-117,231,371 , GRCh37.p13 chr9: 119,884,474-119,993,650 RPL10P3, ASTN2, 3 more genes
    nsv6314063copy number variation1nstd102humanUncertain significance GRCh37 chr9: 119,722,551-121,219,732 , GRCh38.p12 chr9: 116,960,272-118,457,454 LOC101928797, LOC105376237, 14 more genes
    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
    nsv6313908copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,506,015-119,942,279 , GRCh38.p12 chr9: 113,743,735-117,180,000 LOC105376224, TEX53, 45 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 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
    nsv6290238copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,853,848-124,633,077 , GRCh38.p12 chr9: 115,091,569-121,870,798 LINC00474, LOC107987123, 72 more genes
    nsv6136728copy number variation1nstd213human GRCh37 chr9: 117,920,000-120,020,001 , GRCh38.p12 chr9: 115,157,721-117,257,722 LINC00474, SNORA70C, 19 more genes
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
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