U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 491

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147521copy number variation1nstd232human GRCh37.p13 chr9: 139,697,592-139,697,651 , GRCh38.p12 chr9: 136,803,140-136,803,199 CCDC183, CCDC183-AS1
    nsv7146024copy number variation1nstd232human GRCh37.p13 chr9: 139,697,621-139,697,741 , GRCh38.p12 chr9: 136,803,169-136,803,289 CCDC183, CCDC183-AS1
    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
    nsv6887448copy number variation1nstd229human GRCh38 chr9: 136,757,319-137,066,079 , GRCh37.p13 chr9: 139,651,771-139,960,531 LCN8, TMEM141, 31 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
    nsv6450226copy number variation1nstd223human GRCh38 chr9: 136,769,701-136,803,200 , GRCh37.p13 chr9: 139,664,153-139,697,652 CCDC183-AS1, TMEM141, 3 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
    nsv6447606copy number variation1nstd223human GRCh38 chr9: 136,771,001-136,807,700 , GRCh37.p13 chr9: 139,665,453-139,702,152 LOC100422233, CCDC183, 4 more genes
    nsv6444199copy number variation1nstd223human GRCh38 chr9: 136,806,801-136,810,000 , GRCh37.p13 chr9: 139,701,253-139,704,452 CCDC183, CCDC183-AS1, 2 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center