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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5643479insertion1nstd207human GRCh38 chr9: 68,326,648-68,326,648 , GRCh37.p13 chr9|NW_003871067.1: 106,096-106,096 , GRCh37.p13 chr9: 70,941,564-70,941,564 LOC101929800
    nsv5636133insertion1nstd207human GRCh38 chr9: 68,326,815-68,326,815 , GRCh37.p13 chr9: 70,941,731-70,941,731 , GRCh37.p13 chr9|NW_003871067.1: 106,263-106,263 LOC101929800
    nsv5634339insertion1nstd207human GRCh38 chr9: 68,323,178-68,323,178 , GRCh37.p13 chr9: 70,938,094-70,938,094 , GRCh37.p13 chr9|NW_003871067.1: 102,626-102,626 LOC101929800
    nsv5630228insertion1nstd207human GRCh38 chr9: 68,322,808-68,322,808 , GRCh37.p13 chr9: 70,937,724-70,937,724 , GRCh37.p13 chr9|NW_003871067.1: 102,256-102,256 LOC101929800
    nsv5626157insertion1nstd207human GRCh38 chr9: 68,327,332-68,327,332 , GRCh37.p13 chr9: 70,942,248-70,942,248 , GRCh37.p13 chr9|NW_003871067.1: 106,780-106,780 LOC101929800
    nsv5624814insertion1nstd207human GRCh38 chr9: 68,324,236-68,324,236 , GRCh37.p13 chr9: 70,939,152-70,939,152 , GRCh37.p13 chr9|NW_003871067.1: 103,684-103,684 LOC101929800
    nsv5593344copy number variation1nstd207human GRCh38 chr9: 68,322,142-68,327,264 , GRCh37.p13 chr9|NW_003871067.1: 101,590-106,712 , GRCh37.p13 chr9: 70,937,058-70,942,180 LOC101929800
    nsv5591452copy number variation1nstd207human GRCh38 chr9: 68,321,892-68,322,002 , GRCh37.p13 chr9: 70,936,808-70,936,918 , GRCh37.p13 chr9|NW_003871067.1: 101,340-101,450 LOC101929800
    nsv5586293copy number variation1nstd207human GRCh38 chr9: 68,326,485-68,327,135 , GRCh37.p13 chr9: 70,941,401-70,942,051 , GRCh37.p13 chr9|NW_003871067.1: 105,933-106,583 LOC101929800
    nsv5585993copy number variation1nstd207human GRCh38 chr9: 68,322,903-68,322,982 , GRCh37.p13 chr9: 70,937,819-70,937,898 , GRCh37.p13 chr9|NW_003871067.1: 102,351-102,430 LOC101929800
    nsv5585881copy number variation1nstd207human GRCh38 chr9: 68,322,175-68,322,245 , GRCh37.p13 chr9|NW_003871067.1: 101,623-101,693 , GRCh37.p13 chr9: 70,937,091-70,937,161 LOC101929800
    nsv5432626copy number variation1nstd206human GRCh38 chr9: 68,322,324-68,324,269 , GRCh37.p13 chr9: 70,937,240-70,939,185 , GRCh37.p13 chr9|NW_003871067.1: 101,772-103,717 LOC101929800
    nsv5426698copy number variation1nstd206human GRCh38 chr9: 68,315,500-68,320,552 , GRCh37.p13 chr9|NW_003871067.1: 94,948-100,000 , GRCh37.p13 chr9: 70,930,416-70,935,468 LOC101929800
    nsv5258598copy number variation1nstd204human GRCh38.p13 chr9: 68,330,601-68,342,900 , GRCh37.p13 chr9: 70,945,517-70,957,816 , GRCh37.p13 chr9|NW_003871067.1: 110,049-122,348 LOC102723624, LOC101929800
    nsv4744337copy number variation1nstd199human GRCh37 chr9: 70,937,837-70,937,919 , GRCh38.p12 chr9: 68,322,921-68,323,003 LOC101929800
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4644350copy number variation1nstd186human GRCh37 chr9: 70,927,000-70,940,000 , GRCh38.p12 chr9: 68,312,084-68,325,084 LOC101929800, LOC107987077
    nsv4643892copy number variation3nstd186human GRCh37 chr9: 70,927,000-70,942,000 , GRCh38.p12 chr9: 68,312,084-68,327,084 LOC107987077, LOC101929800
    nsv4642196copy number variation1nstd186human GRCh37 chr9: 70,850,150-70,941,300 , GRCh38.p12 chr9: 68,235,234-68,326,384 FOXD4L3, ZNG1C, 2 more genes
    nsv4614896copy number variation1nstd183human GRCh37 chr9: 70,940,595-71,146,533 , GRCh38.p12 chr9: 68,325,679-68,531,617 LOC101929800, PGM5, 3 more genes
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