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Items: 1 to 20 of 611

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098071copy number variation2nstd102humanPathogenic GRCh37 chr9: 139,089,171-141,016,451 , GRCh38.p12 chr9: 136,197,325-138,121,999 NPDC1, LOC101928786, 108 more genes
    nsv7098070copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999 STPG3-AS1, CACNA1B-AS1, 132 more genes
    nsv7098066copy number variation4nstd102humanUncertain significance GRCh37 chr9: 135,139,626-140,034,216 , GRCh38.p12 chr9: 132,264,239-137,139,764 LINC02692, SNORD141A, 181 more genes
    nsv7097704copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,000,557-140,003,043 , GRCh38.p12 chr9: 137,106,105-137,108,591 DPP7, MAN1B1
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7093414copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409 LHX3, FUT7, 121 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7058343inversion1nstd229human GRCh38 chr9: 137,040,737-137,152,702 , GRCh37.p13 chr9: 139,935,189-140,047,154 DPP7, NPDC1, 7 more genes
    nsv6895058copy number variation1nstd229human GRCh38 chr9: 137,077,923-137,094,783 , GRCh37.p13 chr9: 139,972,375-139,989,235 MAN1B1-DT, MAN1B1, 1 more genes
    nsv6888873copy number variation1nstd229human GRCh38 chr9: 136,968,201-137,092,500 , GRCh37.p13 chr9: 139,862,653-139,986,952 CLIC3, SAPCD2, 13 more genes
    nsv6888802copy number variation1nstd229human GRCh38 chr9: 136,947,701-137,099,700 , GRCh37.p13 chr9: 139,842,153-139,994,152 SAPCD2, LCNL1, 14 more genes
    nsv6887241copy number variation1nstd229human GRCh38 chr9: 137,083,533-137,089,032 , GRCh37.p13 chr9: 139,977,985-139,983,484 UAP1L1, MAN1B1, 1 more genes
    nsv6883442copy number variation1nstd229human GRCh38 chr9: 137,040,701-137,148,000 , GRCh37.p13 chr9: 139,935,153-140,042,452 LOC105376327, NPDC1, 7 more genes
    nsv6882911copy number variation1nstd229human GRCh38 chr9: 137,089,249-137,092,917 , GRCh37.p13 chr9: 139,983,701-139,987,369 MAN1B1
    nsv6882129copy number variation1nstd229human GRCh38 chr9: 137,076,177-137,137,592 , GRCh37.p13 chr9: 139,970,629-140,032,044 UAP1L1, MAN1B1, 3 more genes
    nsv6881798copy number variation1nstd229human GRCh38 chr9: 137,072,157-137,132,141 , GRCh37.p13 chr9: 139,966,609-140,026,593 MAN1B1-DT, DPP7, 2 more genes
    nsv6880365copy number variation1nstd229human GRCh38 chr9: 137,050,077-137,135,039 , GRCh37.p13 chr9: 139,944,529-140,029,491 UAP1L1, ENTPD2, 5 more genes
    nsv6880143copy number variation1nstd229human GRCh38 chr9: 137,085,992-137,091,556 , GRCh37.p13 chr9: 139,980,444-139,986,008 MAN1B1-DT, MAN1B1
    nsv6879544copy number variation1nstd229human GRCh38 chr9: 137,077,701-137,112,100 , GRCh37.p13 chr9: 139,972,153-140,006,552 MAN1B1-DT, DPP7, 2 more genes
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