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 156

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099188copy number variation1nstd231human GRCh38.p12 chr1: 27,277,792-27,612,963 , GRCh37 chr1: 27,604,283-27,939,474 FGR, GPR3, 11 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648261copy number variation1nstd229human GRCh38 chr1: 27,610,497-27,610,628 , GRCh37.p13 chr1: 27,937,008-27,937,139 FGR
    nsv6648258copy number variation1nstd229human GRCh38 chr1: 27,439,701-27,781,300 , GRCh37.p13 chr1: 27,766,215-28,107,811 CHMP1AP1, STX12, 11 more genes
    nsv6648256copy number variation1nstd229human GRCh38 chr1: 27,416,201-27,687,300 , GRCh37.p13 chr1: 27,742,695-28,013,811 LINC02574, FGR, 7 more genes
    nsv6648079copy number variation1nstd229human GRCh38 chr1: 27,536,566-27,686,496 , GRCh37.p13 chr1: 27,863,077-28,013,007 LOC729973, RNU6-949P, 5 more genes
    nsv6647641copy number variation1nstd229human GRCh38 chr1: 27,618,116-27,621,221 , GRCh37.p13 chr1: 27,944,627-27,947,732 FGR
    nsv6647354copy number variation1nstd229human GRCh38 chr1: 26,095,901-27,680,900 , GRCh37.p13 chr1: 26,422,392-28,007,411 ZPLD2P, CEP85, 65 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6333556copy number variation1nstd223human GRCh38 chr1: 24,890,501-27,921,300 , GRCh37.p13 chr1: 25,216,992-28,247,811 RUNX3, MACO1, 108 more genes
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 more genes
    nsv5429547copy number variation1nstd206human GRCh38 chr1: 27,306,072-28,001,379 , GRCh37.p13 chr1: 27,632,563-28,327,890 SMPDL3B, SCARNA1, 28 more genes
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5209067copy number variation1nstd204human GRCh38.p13 chr1: 27,087,001-28,123,900 , GRCh37.p13 chr1: 27,413,492-28,450,411 LOC729973, IFI6, 38 more genes
    nsv5202815mobile element deletion1nstd204human GRCh38.p13 chr1: 27,622,015-27,622,311 , GRCh37.p13 chr1: 27,948,526-27,948,822 FGR
    nsv5201015copy number variation1nstd204human GRCh38.p13 chr1: 27,609,401-27,634,100 , GRCh37.p13 chr1: 27,935,912-27,960,611 FGR
    nsv5072231mobile element insertion1nstd203human GRCh38 chr1: 27,630,214-27,630,233 , GRCh37.p13 chr1: 27,956,725-27,956,744 FGR
    nsv5060472mobile element insertion1nstd203human GRCh38 chr1: 27,630,215-27,630,233 , GRCh37.p13 chr1: 27,956,726-27,956,744 FGR
    nsv4772780mobile element deletion1nstd200human GRCh37 chr1: 27,948,535-27,948,814 , GRCh38.p12 chr1: 27,622,024-27,622,303 FGR
    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