U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 40975

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3825681copy number variation1estd219human GRCh37 chr2: 116,727,417-117,419,024 , GRCh38.p12 chr2: 115,969,841-116,661,448 LOC105373576
    esv3860960copy number variation2estd219human GRCh37 chr10: 68,160,377-68,517,719 , GRCh38.p12 chr10: 66,400,619-66,757,961 CTNNA3
    esv3856576copy number variation7estd219human GRCh37 chr9: 11,749,067-12,081,970 , GRCh38.p12 chr9: 11,749,067-12,081,970 LOC101929446
    esv3823320copy number variation1estd219human GRCh37 chr2: 15,164,793-15,488,685 , GRCh38.p12 chr2: 15,024,669-15,348,561 NBAS
    esv3856590copy number variation6estd219human GRCh37 chr9: 11,868,665-12,185,037 , GRCh38.p12 chr9: 11,868,665-12,185,037 LOC105375976
    esv3856575copy number variation7estd219human GRCh37 chr9: 11,731,199-12,017,115 , GRCh38.p12 chr9: 11,731,199-12,017,115 LOC101929446
    esv3837015copy number variation2estd219human GRCh37 chr4: 127,428,048-127,701,663 , GRCh38.p12 chr4: 126,506,893-126,780,508 RBM48P1
    esv3872848copy number variation2estd219human GRCh37 chr14: 46,425,881-46,698,374 , GRCh38.p12 chr14: 45,956,678-46,229,171 LINC00871
    esv3888173copy number variation11estd219human GRCh37 chrX: 6,552,786-6,811,498 , GRCh38.p12 chrX: 6,634,745-6,893,457 PUDP
    esv3846955copy number variation1estd219human GRCh37 chr6: 140,638,722-140,894,926 , GRCh38.p12 chr6: 140,317,585-140,573,789 LOC105378027
    esv3882179copy number variation3estd219human GRCh37 chr18: 64,082,016-64,335,671 , GRCh38.p12 chr18: 66,414,779-66,668,434 CDH19
    esv3832853copy number variation1estd219human GRCh37 chr3: 163,158,528-163,410,210 , GRCh38.p12 chr3: 163,440,740-163,692,422 RNU7-82P
    esv3838270copy number variation2estd219human GRCh37 chr4: 175,944,853-176,191,354 , GRCh38.p12 chr4: 175,023,702-175,270,203 LOC105377552
    esv3841374copy number variation2estd219human GRCh37 chr5: 101,238,922-101,485,197 , GRCh38.p12 chr5: 101,903,218-102,149,493 RNA5SP188
    esv3860964copy number variation3estd219human GRCh37 chr10: 68,170,435-68,402,820 , GRCh38.p12 chr10: 66,410,677-66,643,062 CTNNA3
    esv3885963copy number variation1estd219human GRCh37 chr20: 60,029,277-60,260,972 , GRCh38.p12 chr20: 61,454,221-61,685,916 CDH4
    esv3851286copy number variation1estd219human GRCh37 chr7: 125,839,047-126,063,962 , GRCh38.p12 chr7: 126,198,993-126,423,908 LOC105375488
    esv3888425copy number variation9estd219human GRCh37 chrX: 22,697,248-22,922,088 , GRCh38.p12 chrX: 22,679,131-22,903,971 PTCHD1-AS
    esv3832629copy number variation2estd219human GRCh37 chr3: 154,691,694-154,914,007 , GRCh38.p12 chr3: 154,973,905-155,196,218 MME
    esv3845136copy number variation4estd219human GRCh37 chr6: 68,232,134-68,451,944 , GRCh38.p12 chr6: 67,522,241-67,742,051 , GRCh38.p12 chr6|NW_009646200.1: 1-214,291 RNU6-280P
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

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