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Items: 1 to 20 of 577

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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
    nsv7066875inversion1nstd229human GRCh38 chr9: 136,647,041-136,892,045 , GRCh37.p13 chr9: 139,541,493-139,786,497 DIPK1B, LCN15, 29 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
    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
    nsv6878154copy number variation1nstd229human GRCh38 chr9: 136,649,001-136,652,700 , GRCh37.p13 chr9: 139,543,453-139,547,152 LOC102724193, HSPC324
    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
    nsv6455048copy number variation1nstd223human GRCh38 chr9: 136,652,662-136,653,047 , GRCh37.p13 chr9: 139,547,114-139,547,499 HSPC324, LOC102724193, 1 more genes
    nsv6451546copy number variation1nstd223human GRCh38 chr9: 136,656,508-136,657,520 , GRCh37.p13 chr9: 139,550,960-139,551,972 HSPC324, EGFL7
    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
    nsv6448776copy number variation1nstd223human GRCh38 chr9: 136,577,591-136,723,408 , GRCh37.p13 chr9: 139,472,043-139,617,860 EGFL7, LINC01451, 7 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
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