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 289

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7079661copy number variation1nstd229human GRCh38 chrX: 152,743,133-152,950,602 , GRCh37.p13 chrX|NW_003871103.3: 177,116-384,585 , GRCh37.p13 chrX: 151,958,440-152,119,146 MAGEA2, ZNF185, 7 more genes
    nsv7079660copy number variation1nstd229human GRCh38 chrX: 152,743,001-152,869,400 , GRCh37.p13 chrX|NW_003871103.3: 176,984-303,383 , GRCh37.p13 chrX: 151,958,440-152,037,944 MAGEA6, PSMAGEA, 5 more genes
    nsv7079659copy number variation1nstd229human GRCh38 chrX: 152,739,411-152,907,344 , GRCh37.p13 chrX|NW_003871103.3: 173,394-341,327 , GRCh37.p13 chrX: 151,958,440-152,075,888 MAGEA2, ZNF185, 7 more genes
    nsv7079657copy number variation1nstd229human GRCh38 chrX: 152,735,842-152,928,396 , GRCh37.p13 chrX: 151,958,440-152,096,940 , GRCh37.p13 chrX|NW_003871103.3: 169,825-362,379 NSDHL, CSAG3, 9 more genes
    nsv7079655copy number variation1nstd229human GRCh38 chrX: 152,665,874-152,960,330 , GRCh37.p13 chrX|NW_003871103.3: 99,857-394,313 , GRCh37.p13 chrX: 151,834,345-152,128,874 MAGEA3, LOC105373372, 15 more genes
    nsv7079616copy number variation1nstd229human GRCh38 chrX: 152,264,528-152,792,675 , GRCh37.p13 chrX: 151,433,000-151,734,489 CSAG2, MAGEA2, 17 more genes
    nsv7057941inversion1nstd229human GRCh38 chrX: 152,675,413-152,794,779 , GRCh37.p13 chrX|NW_003871103.3: 109,396-228,762 MAGEA3, MAGEA6, 11 more genes
    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
    nsv7050820inversion1nstd229human GRCh38 chrX: 143,987,812-153,050,091 , GRCh37.p13 chrX|NW_004070890.2: 1-6,530,008 , GRCh37.p13 chrX: 143,070,918-152,218,449 FMR1NB, MIR4330, 139 more genes
    nsv7050106inversion1nstd229human GRCh38 chrX: 152,727,074-152,847,313 , GRCh37.p13 chrX|NW_003871103.3: 161,057-281,296 , GRCh37.p13 chrX: 151,847,041-151,909,928 MAGEA2, CETN2, 8 more genes
    nsv7048245inversion1nstd229human GRCh38 chrX: 152,742,942-152,790,105 , GRCh37.p13 chrX: 151,847,041-151,894,019 , GRCh37.p13 chrX|NW_003871103.3: 176,925-224,088 MAGEA2, PSMAGEA, 3 more genes
    nsv7046711inversion1nstd229human GRCh38 chrX: 145,641,090-152,809,888 , GRCh37.p13 chrX: 144,722,608-151,978,420 , GRCh37.p13 chrX|NW_004070890.2: 1,165,481-6,530,008 FMR1-AS1, LOC100420321, 126 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
    nsv7041676inversion1nstd229human GRCh38 chrX: 152,678,626-152,860,413 , GRCh37.p13 chrX|NW_003871103.3: 112,609-294,396 , GRCh37.p13 chrX: 151,847,041-151,958,394 CSAG3, NSDHL, 13 more genes
    nsv6636982copy number variation1nstd102humanUncertain significance GRCh37 chrX: 151,869,765-152,101,001 , GRCh38.p12 chrX: 152,701,287-152,932,457 CETN2, CSAG4, 13 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634391copy number variation1nstd102humanPathogenic GRCh37 chrX: 142,401,540-155,233,731 , GRCh38.p12 chrX: 143,313,746-156,004,066 CSAG4, LOC112268308, 279 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    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