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Items: 1 to 20 of 257

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv7077264inversion1nstd229human GRCh38 chr9: 107,230,971-107,507,293 , GRCh37.p13 chr9: 109,993,252-110,269,574 RAD23B, LOC107987110, 6 more genes
    nsv7074978inversion1nstd229human GRCh38 chr9: 106,755,903-108,407,110 , GRCh37.p13 chr9: 109,518,184-111,169,390 LOC105376209, LINC01509, 31 more genes
    nsv6875807copy number variation1nstd229human GRCh38 chr9: 107,286,183-107,290,133 , GRCh37.p13 chr9: 110,048,464-110,052,414 RAD23B
    nsv6874656copy number variation1nstd229human GRCh38 chr9: 107,311,687-107,311,833 , GRCh37.p13 chr9: 110,073,968-110,074,114 RAD23B
    nsv6869815copy number variation1nstd229human GRCh38 chr9: 107,284,387-107,291,237 , GRCh37.p13 chr9: 110,046,668-110,053,518 RAD23B
    nsv6865069copy number variation1nstd229human GRCh38 chr9: 107,292,101-107,294,400 , GRCh37.p13 chr9: 110,054,382-110,056,681 RAD23B
    nsv6862856copy number variation1nstd229human GRCh38 chr9: 107,325,004-107,329,543 , GRCh37.p13 chr9: 110,087,285-110,091,824 RAD23B
    nsv6861707copy number variation1nstd229human GRCh38 chr9: 107,263,358-107,282,992 , GRCh37.p13 chr9: 110,025,639-110,045,273 RAD23B
    nsv6859060copy number variation1nstd229human GRCh38 chr9: 107,289,528-107,295,665 , GRCh37.p13 chr9: 110,051,809-110,057,946 RAD23B
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6573610inversion1nstd223human GRCh38 chr9: 107,308,189-107,309,969 , GRCh37.p13 chr9: 110,070,470-110,072,250 RAD23B
    nsv6565040inversion1nstd223human GRCh38 chr9: 107,308,275-107,309,786 , GRCh37.p13 chr9: 110,070,556-110,072,067 RAD23B
    nsv6451826copy number variation1nstd223human GRCh38 chr9: 107,284,387-107,291,234 , GRCh37.p13 chr9: 110,046,668-110,053,515 RAD23B
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 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
    nsv6290765copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,858,276-110,624,997 , GRCh38.p12 chr9: 100,095,994-107,862,716 RNF20, SMC2, 120 more genes
    nsv6268419copy number variation1nstd214human GRCh38 chr9: 107,293,084-107,293,133 , GRCh37.p13 chr9: 110,055,365-110,055,414 RAD23B
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