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 3476

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3836185copy number variation1estd219human GRCh37 chr4: 93,777,871-93,874,952 , GRCh38.p12 chr4: 92,856,720-92,953,801 GRID2
    esv3860275copy number variation131estd219human GRCh37 chr10: 38,818,427-38,907,931 , GRCh38.p12 chr10: 38,529,499-38,614,800 ABCD1P2
    esv3872670copy number variation646estd219human GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445 LINC02315
    esv3853507copy number variation1095estd219human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3836193copy number variation2estd219human GRCh37 chr4: 93,862,122-93,893,631 , GRCh38.p12 chr4: 92,940,971-92,972,480 GRID2
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3864714copy number variation1estd219human GRCh37 chr11: 81,908,879-81,929,788 , GRCh38.p12 chr11: 82,197,837-82,218,746 MIR4300HG
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3836195copy number variation5estd219human GRCh37 chr4: 93,894,901-93,913,512 , GRCh38.p12 chr4: 92,973,750-92,992,361 GRID2
    esv3874935copy number variation3estd219human GRCh37 chr15: 44,423,546-44,440,859 , GRCh38.p12 chr15: 44,131,348-44,148,661 FRMD5
    esv3836186copy number variation1estd219human GRCh37 chr4: 93,780,295-93,796,974 , GRCh38.p12 chr4: 92,859,144-92,875,823 GRID2
    esv3872240copy number variation108estd219human GRCh37 chr14: 24,449,758-24,464,787 , GRCh38.p12 chr14: 23,980,549-23,995,578 , GRCh38.p12 chr14|NW_018654722.1: 286,883-301,912 DHRS4L2
    esv3864715copy number variation2estd219human GRCh37 chr11: 81,909,196-81,923,697 , GRCh38.p12 chr11: 82,198,154-82,212,655 MIR4300HG
    esv3851465copy number variation1169estd219human GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
    esv3878137copy number variation1122estd219human GRCh37 chr16: 78,371,328-78,385,326 , GRCh38.p12 chr16: 78,337,431-78,351,429 WWOX
    esv3850618copy number variation797estd219human GRCh37 chr7: 100,327,251-100,341,280 , GRCh38.p12 chr7: 100,729,628-100,743,657 ZAN
    esv3852899copy number variation131estd219human GRCh37 chr8: 15,401,164-15,415,291 , GRCh38.p12 chr8: 15,543,655-15,557,782 TUSC3
    esv3842787copy number variation424estd219human GRCh37 chr5: 155,475,886-155,488,649 , GRCh38.p12 chr5: 156,048,876-156,061,639 SGCD
    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