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Items: 1 to 20 of 392

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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
    nsv7077226inversion1nstd229human GRCh38 chr9: 136,316,295-136,475,130 , GRCh37.p13 chr9: 139,252,829-139,369,582 ENTR1, GPSM1, 7 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
    nsv7069792inversion1nstd229human GRCh38 chr9: 136,285,122-136,523,179 , GRCh37.p13 chr9: 139,252,829-139,417,631 NOTCH1, DKFZP434A062, 11 more genes
    nsv7064509inversion1nstd229human GRCh38 chr9: 136,361,293-136,367,601 , GRCh37.p13 chr9: 139,255,745-139,262,053 CARD9, DNLZ
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6896412copy number variation1nstd229human GRCh38 chr9: 136,363,898-136,387,788 , GRCh37.p13 chr9: 139,258,350-139,282,240 CARD9, SNAPC4, 1 more genes
    nsv6892276copy number variation1nstd229human GRCh38 chr9: 136,362,098-136,384,016 , GRCh37.p13 chr9: 139,256,550-139,278,468 SNAPC4, DNLZ, 1 more genes
    nsv6887498copy number variation1nstd229human GRCh38 chr9: 136,214,667-136,443,437 , GRCh37.p13 chr9: 139,106,513-139,337,889 DKFZP434A062, QSOX2, 9 more genes
    nsv6886252copy number variation1nstd229human GRCh38 chr9: 136,360,037-136,362,826 , GRCh37.p13 chr9: 139,254,489-139,257,278 CARD9, DNLZ, 1 more genes
    nsv6886124copy number variation1nstd229human GRCh38 chr9: 136,285,101-136,404,200 , GRCh37.p13 chr: NaN-NaN GPSM1, SNAPC4, 5 more genes
    nsv6884635copy number variation1nstd229human GRCh38 chr9: 136,359,130-136,362,841 , GRCh37.p13 chr9: 139,253,582-139,257,293 CARD9, GPSM1, 1 more genes
    nsv6884507copy number variation1nstd229human GRCh38 chr9: 135,999,993-136,390,538 , GRCh37.p13 chr9: 138,891,839-139,284,990 LINC02846, CCDC187, 10 more genes
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