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 310

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148249copy number variation1nstd102humanPathogenic GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322 TRDN-AS1, LOC100420743, 179 more genes
    nsv7138566insertion1nstd232human GRCh37.p13 chr6: 127,282,685-127,282,685 , GRCh38.p12 chr6: 126,961,540-126,961,540 LOC105377989
    nsv7054647inversion1nstd229human GRCh38 chr6: 125,609,155-134,343,808 , GRCh37.p13 chr6: 125,930,301-134,664,946 RPS12, TMEM244, 130 more genes
    nsv7053719inversion1nstd229human GRCh38 chr6: 125,606,974-134,343,957 , GRCh37.p13 chr6: 125,928,120-134,665,095 SNORD100, SLC18B1, 130 more genes
    nsv7051513inversion1nstd229human GRCh38 chr6: 126,979,413-127,005,522 , GRCh37.p13 chr6: 127,300,558-127,326,667 LOC105377989
    nsv7047931inversion1nstd229human GRCh38 chr6: 126,975,894-127,005,493 , GRCh37.p13 chr6: 127,297,039-127,326,638 LOC105377989
    nsv7042981inversion1nstd229human GRCh38 chr6: 122,939,434-128,158,341 , GRCh37.p13 chr6: 123,260,579-128,479,486 CENPW, VIM2P, 56 more genes
    nsv7038109inversion1nstd229human GRCh38 chr6: 125,606,921-134,343,957 , GRCh37.p13 chr6: 125,928,067-134,665,095 PTPRK-AS1, MED23, 130 more genes
    nsv6817012copy number variation1nstd229human GRCh38 chr6: 126,976,511-126,976,774 , GRCh37.p13 chr6: 127,297,656-127,297,919 LOC105377989
    nsv6814567copy number variation1nstd229human GRCh38 chr6: 126,977,952-127,090,279 , GRCh37.p13 chr6: 127,299,097-127,411,424 LOC105377989
    nsv6814533copy number variation1nstd229human GRCh38 chr6: 126,923,203-126,925,121 , GRCh37.p13 chr6: 127,244,348-127,246,266 LOC105377989
    nsv6814392copy number variation1nstd229human GRCh38 chr6: 126,942,028-126,947,525 , GRCh37.p13 chr6: 127,263,173-127,268,670 LOC105377989
    nsv6812580copy number variation1nstd229human GRCh38 chr6: 126,939,342-126,942,880 , GRCh37.p13 chr6: 127,260,487-127,264,025 LOC105377989
    nsv6810779copy number variation1nstd229human GRCh38 chr6: 126,843,496-126,951,781 , GRCh37.p13 chr6: 127,164,641-127,272,926 LOC105377989, LOC105377991
    nsv6810735copy number variation1nstd229human GRCh38 chr6: 126,984,549-126,990,917 , GRCh37.p13 chr6: 127,305,694-127,312,062 LOC105377989
    nsv6810568copy number variation1nstd229human GRCh38 chr6: 126,888,201-126,894,300 , GRCh37.p13 chr6: 127,209,346-127,215,445 LOC105377989
    nsv6808883copy number variation1nstd229human GRCh38 chr6: 126,865,722-126,890,819 , GRCh37.p13 chr6: 127,186,867-127,211,964 LOC105377991, LOC105377989
    nsv6808747copy number variation1nstd229human GRCh38 chr6: 126,943,017-126,951,584 , GRCh37.p13 chr6: 127,264,162-127,272,729 LOC105377989
    nsv6807906copy number variation1nstd229human GRCh38 chr6: 126,989,285-127,003,811 , GRCh37.p13 chr6: 127,310,430-127,324,956 LOC105377989
    nsv6807766copy number variation1nstd229human GRCh38 chr6: 126,937,801-126,963,230 , GRCh37.p13 chr6: 127,258,946-127,284,375 LOC105377989
    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