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 416

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148061copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,217,915-153,618,382 , GRCh38.p12 chrX: 153,952,464-154,390,022 MIR3202-1, LOC105373386, 18 more genes
    nsv7148059copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,247,464-153,522,710 , GRCh38.p12 chrX: 153,982,013-154,294,356 TEX28, OPN1MW, 11 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098869copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,586,015-154,774,957 , GRCh38.p12 chrX: 140,503,850-155,545,296 MAGEA6, LOC101928832, 303 more genes
    nsv7098599copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,001,546-154,563,736 , GRCh38.p12 chrX: 153,736,092-155,334,427 TAFAZZIN, LOC105373386, 82 more genes
    nsv7098350copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,195,397-153,642,547 , GRCh38.p12 chrX: 153,929,944-154,414,210 TKTL1, IRAK1, 24 more genes
    nsv7098237copy number variation3nstd102humanUncertain significance GRCh37 chrX: 153,195,397-153,583,460 , GRCh38.p12 chrX: 153,929,944-154,355,092 OPN1MW2, TEX28, 19 more genes
    nsv7098006copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,357,622-153,664,237 , GRCh38.p12 chrX: 154,092,164-154,435,891 EMD, FLNA, 18 more genes
    nsv7098002copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,128,118-153,664,237 , GRCh38.p12 chrX: 153,862,663-154,435,891 OPN1MW, TEX28, 31 more genes
    nsv7097996copy number variation6nstd102humanPathogenic GRCh37 chrX: 152,014,869-155,171,615 , GRCh38.p12 chrX: 152,846,325-155,941,951 PHF10P1, ZNF185, 132 more genes
    nsv7097995copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 152,014,869-154,563,736 , GRCh38.p12 chrX: 152,846,325-155,334,427 RN7SL697P, CYCSP45, 118 more genes
    nsv7079879copy number variation1nstd229human GRCh38 chrX: 154,324,201-154,504,700 , GRCh37.p13 chrX: 153,552,547-153,733,031 , GRCh37.p13 chrX|NW_003871103.3: 1,758,180-1,938,679 LAGE3, FLNA, 17 more genes
    nsv7079878copy number variation1nstd229human GRCh38 chrX: 154,309,633-154,536,356 , GRCh37.p13 chrX|NW_003871103.3: 1,743,612-1,970,335 , GRCh37.p13 chrX: 153,537,985-153,764,571 SNORA70, LOC105373386, 18 more genes
    nsv7079877copy number variation1nstd229human GRCh38 chrX: 154,302,235-154,302,278 , GRCh37.p13 chrX|NW_003871103.3: 1,736,214-1,736,257 , GRCh37.p13 chrX: 153,530,586-153,530,629 TKTL1
    nsv7057928inversion1nstd229human GRCh38 chrX: 152,528,769-155,098,506 , GRCh37.p13 chrX: 151,734,490-154,326,781 , GRCh37.p13 chrX|NW_003871103.3: 1-2,532,485 F8, ATP6AP1, 128 more genes
    nsv7051950inversion1nstd229human GRCh38 chrX: 153,712,302-154,514,525 , GRCh37.p13 chrX: 152,977,757-153,742,849 , GRCh37.p13 chrX|NW_003871103.3: 1,146,285-1,948,504 MIR3202-1, LAGE3, 48 more genes
    nsv7047108inversion1nstd229human GRCh38 chrX: 153,824,232-154,611,904 , GRCh37.p13 chrX: 153,089,687-153,840,157 , GRCh37.p13 chrX|NW_003871103.3: 1,258,215-2,045,883 HCFC1, SNORA70, 46 more genes
    nsv7046320inversion1nstd229human GRCh38 chrX: 152,800,888-155,032,704 , GRCh37.p13 chrX|NW_003871103.3: 234,871-2,466,683 , GRCh37.p13 chrX: 151,969,427-154,260,979 FUNDC2, PNCK, 111 more genes
    nsv7046188inversion1nstd229human GRCh38 chrX: 152,545,731-155,311,806 , GRCh37.p13 chrX: 151,734,490-154,541,118 , GRCh37.p13 chrX|NW_003871103.3: 1-2,745,785 TEX28, SSR4, 133 more genes
    nsv7040390inversion1nstd229human GRCh38 chrX: 154,311,629-154,311,717 , GRCh37.p13 chrX|NW_003871103.3: 1,745,608-1,745,696 , GRCh37.p13 chrX: 153,539,980-153,540,068 TKTL1
    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