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 206

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 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
    nsv7097932copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,884,602-135,942,612 , GRCh38.p12 chr9: 131,009,215-133,067,225 LAMC3, SPACA9, 40 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
    nsv7069969inversion1nstd229human GRCh38 chr9: 133,053,027-133,053,456 , GRCh37.p13 chr9: 135,928,414-135,928,843 GTF3C5
    nsv7064617inversion1nstd229human GRCh38 chr9: 133,025,311-133,029,600 , GRCh37.p13 chr9: 135,900,698-135,904,987 LOC105376306, GTF3C5
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6876313copy number variation1nstd229human GRCh38 chr9: 133,042,148-133,046,904 , GRCh37.p13 chr9: 135,917,535-135,922,291 GTF3C5
    nsv6874955copy number variation1nstd229human GRCh38 chr9: 133,032,516-133,038,215 , GRCh37.p13 chr9: 135,907,903-135,913,602 GTF3C5
    nsv6872123copy number variation1nstd229human GRCh38 chr9: 133,032,501-133,037,700 , GRCh37.p13 chr9: 135,907,888-135,913,087 GTF3C5
    nsv6871490copy number variation1nstd229human GRCh38 chr9: 133,025,701-133,034,500 , GRCh37.p13 chr9: 135,901,088-135,909,887 LOC105376306, GTF3C5
    nsv6870007copy number variation1nstd229human GRCh38 chr9: 132,916,912-133,049,166 , GRCh37.p13 chr9: 135,792,299-135,924,553 SNORD141A, MIR548AW, 7 more genes
    nsv6869503copy number variation1nstd229human GRCh38 chr9: 133,032,101-133,037,800 , GRCh37.p13 chr9: 135,907,488-135,913,187 GTF3C5
    nsv6867476copy number variation1nstd229human GRCh38 chr9: 133,032,442-133,038,109 , GRCh37.p13 chr9: 135,907,829-135,913,496 GTF3C5
    nsv6863433copy number variation1nstd229human GRCh38 chr9: 133,014,701-133,035,800 , GRCh37.p13 chr9: 135,890,088-135,911,187 GTF3C5, EEF1A1P5, 2 more genes
    nsv6637649copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,354,006-135,950,908 , GRCh38.p12 chr9: 132,478,619-133,075,521 GFI1B, SNORD141A, 15 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
    nsv6454541copy number variation1nstd223human GRCh38 chr9: 133,027,143-133,038,647 , GRCh37.p13 chr9: 135,902,530-135,914,034 GTF3C5, LOC105376306
    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