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Items: 1 to 20 of 459

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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
    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
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6896738copy number variation1nstd229human GRCh38 chr9: 136,983,001-136,985,800 , GRCh37.p13 chr9: 139,877,453-139,880,252 LCNL1
    nsv6891849copy number variation1nstd229human GRCh38 chr9: 136,961,001-137,005,021 , GRCh37.p13 chr9: 139,855,453-139,899,473 PAXX, LINC02692, 3 more genes
    nsv6889752copy number variation1nstd229human GRCh38 chr9: 136,982,090-136,985,904 , GRCh37.p13 chr9: 139,876,542-139,880,356 PTGDS, LCNL1
    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
    nsv6887448copy number variation1nstd229human GRCh38 chr9: 136,757,319-137,066,079 , GRCh37.p13 chr9: 139,651,771-139,960,531 LCN8, TMEM141, 31 more genes
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6450572copy number variation1nstd223human GRCh38 chr9: 135,800,101-137,359,000 , GRCh37.p13 chr9: 138,691,947-140,253,452 LCN6, PAXX, 96 more genes
    nsv6448504copy number variation1nstd223human GRCh38 chr9: 135,900,001-137,301,100 , GRCh37.p13 chr9: 138,791,847-140,195,552 DIPK1B, LOC105376326, 95 more genes
    nsv6445851copy number variation1nstd223human GRCh38 chr9: 136,986,051-136,999,549 , GRCh37.p13 chr9: 139,880,503-139,894,001 CLIC3, LCNL1, 1 more genes
    nsv6313986copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,563,039-140,310,033 , GRCh38.p12 chr9: 136,668,587-137,415,581 RABL6, ANAPC2, 68 more genes
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