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 107

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2757428copy number variation6estd1human NCBI35 chr11: 21,112,669-21,194,273 , GRCh37.p13 chr11: 21,156,093-21,237,697 , GRCh38.p12 chr11: 21,134,547-21,216,151 NELL1
    esv2756816copy number variation33estd1human NCBI35 chr16: 79,529,780-79,584,643 , GRCh37.p13 chr16: 80,972,279-81,027,142 , GRCh38.p12 chr16: 80,938,382-80,993,537 CMC2
    esv2757518copy number variation2estd1human NCBI35 chr12: 125,324,021-125,362,245 , GRCh37.p13 chr12|NW_003315940.1: 87,388-131,664 , GRCh37.p13 chr12: 126,799,141-126,837,365 , GRCh38.p12 chr12: 126,314,595-126,352,819 , GRCh38.p12 chr12|NW_003315940.1: 87,388-131,664 LOC105379613
    esv2756883copy number variation4estd1human NCBI35 chr1: 206,967,918-207,009,174 , GRCh37.p13 chr1: 210,579,523-210,620,779 , GRCh38.p12 chr1: 210,406,179-210,447,435 , GRCh38.p12 chr1|NW_011332687.1: 185,921-227,177 HHAT
    esv2757596copy number variation1estd1human NCBI35 chr15: 32,688,453-32,729,249 , GRCh37.p13 chr15: 34,901,161-34,941,957 , GRCh38.p12 chr15: 34,608,960-34,649,756 LINC02252
    esv2757666copy number variation3estd1human NCBI35 chr18: 277,648-306,558 , GRCh37.p13 chr18: 287,648-316,558 , GRCh38.p12 chr18: 287,648-316,558 COLEC12
    esv2757261copy number variation2estd1human NCBI35 chr8: 14,300,858-14,321,648 , GRCh37.p13 chr8: 14,256,487-14,277,277 , GRCh38.p12 chr8: 14,398,978-14,419,768 SGCZ
    esv2757561copy number variation2estd1human NCBI35 chr14: 40,541,848-40,562,301 , GRCh37.p13 chr14: 41,472,098-41,492,551 , GRCh38.p12 chr14: 41,002,893-41,023,346 LINC02315
    esv2757787copy number variation190estd1human GRCh38.p12 chr2: 22,591,267-22,897,147 , NCBI35 chr2: 22,725,791-23,031,671 , GRCh37.p13 chr2: 22,814,139-23,120,019 RN7SKP27
    esv2758513copy number variation6estd1human NCBI35 chr20: 10,840,138-11,064,725 , GRCh37.p13 chr20: 10,892,138-11,116,725 , GRCh38.p12 chr20: 10,911,490-11,136,077 LINC02871
    esv2758280copy number variation39estd1human NCBI35 chr11: 88,083,993-88,339,832 , GRCh37.p13 chr11: 88,444,345-88,700,184 , GRCh38.p12 chr11: 88,711,177-88,967,016 GRM5
    esv2758166copy number variation9estd1human GRCh38.p12 chr8: 99,016,620-99,184,453 , NCBI35 chr8: 100,098,024-100,265,857 , GRCh37.p13 chr8: 100,028,848-100,196,681 VPS13B
    esv2757774copy number variation69estd1human NCBI35 chr1: 221,711,686-221,833,513 , GRCh38.p12 chr1: 225,217,249-225,339,076 , GRCh37.p13 chr1: 225,404,951-225,526,778 DNAH14
    esv2757951copy number variation95estd1human GRCh38.p12 chr4: 116,601,155-116,699,723 , GRCh37.p13 chr4: 117,522,311-117,620,879 , NCBI35 chr4: 117,879,914-117,978,482 LOC105377385
    esv2757086copy number variation22estd1human GRCh38.p12 chr4: 151,855,119-151,888,586 , GRCh37.p13 chr4: 152,776,271-152,809,738 , NCBI35 chr4: 153,133,876-153,167,343 LOC102724700, LOC105377488
    esv2757029copy number variation2estd1human GRCh37.p13 chr3: 197,290,158-197,319,822 , GRCh38.p12 chr3: 197,563,287-197,592,951 , NCBI35 chr3: 198,778,468-198,808,132 BDH1, RPL36P7
    esv2757967copy number variation264estd1human GRCh38.p12 chr4: 167,813,440-168,130,542 , GRCh37.p13 chr4: 168,734,591-169,051,693 , NCBI35 chr4: 169,109,321-169,426,423 ANXA10, LOC105377523
    esv2758017copy number variation102estd1human NCBI35 chr5: 130,466,896-130,619,811 , GRCh37.p13 chr5: 130,438,997-130,591,912 , GRCh38.p12 chr5: 131,103,304-131,256,219 HINT1, LYRM7
    esv2758569copy number variation74estd1human NCBI35 chrX: 56,622,090-56,770,769 , GRCh37.p13 chrX: 56,739,069-56,887,748 , GRCh38.p12 chrX: 56,712,636-56,861,315 UQCRBP1, NBDY
    esv2757168copy number variation4estd1human GRCh38.p12 chr6: 52,928,056-52,996,406 , NCBI35 chr6: 52,900,813-52,969,163 , GRCh37.p13 chr6: 52,792,854-52,861,204 GSTA4, RN7SK, 1 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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