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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138094copy number variation1nstd232human GRCh37.p13 chr9: 140,136,280-140,136,360 , GRCh38.p12 chr9: 137,241,828-137,241,908 TUBB4B, CIMIP2A
    nsv7098440copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,036,445-140,138,008 , GRCh38.p12 chr9: 137,141,993-137,243,556 SSNA1, CYSRT1, 14 more genes
    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
    nsv7097938copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 140,040,158-141,016,451 , GRCh38.p12 chr9: 137,145,706-138,121,999 NELFB, LOC651337, 39 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
    nsv7068117inversion1nstd229human GRCh38 chr9: 137,246,535-138,000,327 , GRCh37.p13 chr9: 140,140,987-140,894,779 NELFB, MIR7114, 23 more genes
    nsv6897081copy number variation1nstd229human GRCh38 chr9: 137,175,201-137,279,700 , GRCh37.p13 chr9: 140,069,653-140,174,152 SLC34A3, TOR4A, 13 more genes
    nsv6894329copy number variation1nstd229human GRCh38 chr9: 137,233,101-137,254,600 , GRCh37.p13 chr9: 140,127,553-140,149,052 NELFB, TUBB4B, 4 more genes
    nsv6891571copy number variation1nstd229human GRCh38 chr9: 137,242,065-137,242,517 , GRCh37.p13 chr9: 140,136,517-140,136,969 CIMIP2A, TUBB4B
    nsv6890682copy number variation1nstd229human GRCh38 chr9: 137,243,960-137,244,010 , GRCh37.p13 chr9: 140,138,412-140,138,462 CIMIP2A, TUBB4B
    nsv6884802copy number variation1nstd229human GRCh38 chr9: 137,242,217-137,252,925 , GRCh37.p13 chr9: 140,136,669-140,147,377 TUBB4B, STPG3, 2 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
    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
    nsv6313935copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,740,078-141,020,389 , GRCh38.p12 chr9: 135,848,232-138,125,937 ENTR1, LINC02692, 115 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
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