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Items: 1 to 20 of 402

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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
    nsv7070027inversion1nstd229human GRCh38 chr9: 135,876,745-136,834,735 , GRCh37.p13 chr9: 138,768,591-139,729,187 LOC107987142, LCN8, 48 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
    nsv7058128inversion1nstd229human GRCh38 chr9: 136,404,238-136,577,692 , GRCh37.p13 chr9: 139,298,690-139,472,144 NOTCH1, INPP5E, 7 more genes
    nsv6896430copy number variation1nstd229human GRCh38 chr9: 136,543,951-136,657,540 , GRCh37.p13 chr9: 139,438,403-139,551,992 LOC102724193, NALT1, 6 more genes
    nsv6894711copy number variation1nstd229human GRCh38 chr9: 136,548,601-136,557,100 , GRCh37.p13 chr9: 139,443,053-139,451,552 NALT1
    nsv6887039copy number variation1nstd229human GRCh38 chr9: 136,549,730-136,557,129 , GRCh37.p13 chr9: 139,444,182-139,451,581 NALT1
    nsv6886459copy number variation1nstd229human GRCh38 chr9: 136,523,101-136,577,700 , GRCh37.p13 chr9: 139,417,553-139,472,152 NOTCH1, NALT1, 1 more genes
    nsv6637382copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,307,719-139,563,040 , GRCh38.p12 chr9: 136,413,267-136,668,588 MIR4673, PMPCA, 11 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
    nsv6442484copy number variation1nstd223human GRCh38 chr9: 136,549,730-136,557,125 , GRCh37.p13 chr9: 139,444,182-139,451,577 NALT1
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