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 272

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098753copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 135,777,087-135,777,160 , GRCh38 chr9: 132,901,700-132,901,773 TSC1
    nsv7098431copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,775,735-135,866,437 , GRCh38.p12 chr9: 132,900,348-132,991,050 RPL39P24, TSC1, 3 more genes
    nsv7098430copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,771,622-135,773,017 , GRCh38.p12 chr9: 132,896,235-132,897,630 TSC1
    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
    nsv7098067copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,798,715-135,798,899 , GRCh38.p12 chr9: 132,923,328-132,923,512 TSC1
    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
    nsv7097935copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,820,391-135,821,434 , GRCh38.p12 chr9: 132,945,004-132,946,047 TSC1, GFI1B, 1 more genes
    nsv7097934copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,771,184-135,781,738 , GRCh38.p12 chr9: 132,895,797-132,906,351 TSC1
    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
    nsv7093444delins1nstd102humanPathogenic GRCh37 chr9: 135,781,310-135,781,311 , GRCh38 chr9: 132,905,923-132,905,924 TSC1
    nsv7076265inversion1nstd229human GRCh38 chr9: 132,902,384-132,906,971 , GRCh37.p13 chr9: 135,777,771-135,782,358 TSC1
    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
    nsv6871526copy number variation1nstd229human GRCh38 chr9: 132,902,819-132,908,728 , GRCh37.p13 chr9: 135,778,206-135,784,115 TSC1
    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
    nsv6866176copy number variation1nstd229human GRCh38 chr9: 132,944,966-132,950,750 , GRCh37.p13 chr9: 135,820,353-135,826,137 TSC1, GFI1B, 1 more genes
    nsv6864467copy number variation1nstd229human GRCh38 chr9: 132,432,101-132,918,100 , GRCh37.p13 chr9: 135,307,488-135,793,487 TSC1, GTF3C4, 5 more genes
    nsv6861158copy number variation1nstd229human GRCh38 chr9: 132,891,001-132,894,200 , GRCh37.p13 chr9: 135,766,388-135,769,587 TSC1
    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