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Items: 1 to 20 of 323

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142515copy number variation1nstd232human GRCh37.p13 chr9: 135,981,223-135,981,282 , GRCh38.p12 chr9: 133,105,836-133,105,895 RALGDS
    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
    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
    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
    nsv6876524copy number variation1nstd229human GRCh38 chr9: 133,102,359-133,102,389 , GRCh37.p13 chr9: 135,977,746-135,977,776 RALGDS
    nsv6876413copy number variation1nstd229human GRCh38 chr9: 133,078,801-133,132,100 , GRCh37.p13 chr9: 135,954,188-136,007,487 CELP, RALGDS
    nsv6876230copy number variation1nstd229human GRCh38 chr9: 133,145,482-133,145,518 , GRCh37.p13 chr9: 136,020,869-136,020,905 RALGDS
    nsv6874163copy number variation1nstd229human GRCh38 chr9: 133,113,888-133,115,810 , GRCh37.p13 chr9: 135,989,275-135,991,197 RALGDS
    nsv6870884copy number variation1nstd229human GRCh38 chr9: 133,143,519-133,152,809 , GRCh37.p13 chr9: 136,018,906-136,028,196 RALGDS, GBGT1
    nsv6867699copy number variation1nstd229human GRCh38 chr9: 133,145,401-133,151,000 , GRCh37.p13 chr9: 136,020,788-136,026,387 RALGDS, GBGT1
    nsv6863624copy number variation1nstd229human GRCh38 chr9: 133,096,537-133,102,992 , GRCh37.p13 chr9: 135,971,924-135,978,379 RALGDS
    nsv6862369copy number variation1nstd229human GRCh38 chr9: 133,119,978-133,123,523 , GRCh37.p13 chr9: 135,995,365-135,998,910 RALGDS
    nsv6861178copy number variation1nstd229human GRCh38 chr9: 133,130,263-133,131,273 , GRCh37.p13 chr9: 136,005,650-136,006,660 RALGDS
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6451897copy number variation1nstd223human GRCh38 chr9: 133,123,693-133,124,146 , GRCh37.p13 chr9: 135,999,080-135,999,533 RALGDS
    nsv6436211copy number variation1nstd223human GRCh38 chr9: 133,129,998-133,132,748 , GRCh37.p13 chr9: 136,005,385-136,008,135 RALGDS
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6268411copy number variation1nstd214human GRCh38 chr9: 133,105,848-133,105,907 , GRCh37.p13 chr9: 135,981,235-135,981,294 RALGDS
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