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 353

    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
    nsv7099016copy number variation1nstd102humanLikely benign GRCh37 chrX: 148,563,634-148,862,206 , GRCh38.p12 chrX: 149,482,103-149,780,543 EOLA1, LOC100420334, 14 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
    nsv7098783copy number variation1nstd102humanLikely benign GRCh37 chrX: 148,564,275-148,798,438 , GRCh38.p12 chrX: 149,482,744-149,716,778 IDS2, HSFX3, 9 more genes
    nsv7085366copy number variation1nstd229human GRCh38 chrX: 149,548,001-149,548,500 , GRCh37.p13 chrX|NW_004070890.2: 5,072,399-5,072,898 , GRCh37.p13 chrX: 148,629,546-148,630,045 EOLA1, HSFX3
    nsv7085363copy number variation1nstd229human GRCh38 chrX: 149,524,501-149,540,000 , GRCh37.p13 chrX|NW_004070890.2: 5,048,899-5,064,398 , GRCh37.p13 chrX: 148,606,040-148,621,560 IDS2, IDSP1, 2 more genes
    nsv7085345copy number variation1nstd229human GRCh38 chrX: 149,378,771-149,699,527 , GRCh37.p13 chrX|NW_004070890.2: 4,903,168-5,223,925 , GRCh37.p13 chrX: 148,460,301-148,781,187 MAGEA9B, LOC107985667, 10 more genes
    nsv7055224inversion1nstd229human GRCh38 chrX: 149,372,897-150,622,533 , GRCh37.p13 chrX: 148,454,427-149,791,006 , GRCh37.p13 chrX|NW_004070890.2: 4,897,294-6,146,931 HSFX1, LOC100420322, 28 more genes
    nsv7052723inversion1nstd229human GRCh38 chrX: 149,384,651-149,611,710 , GRCh37.p13 chrX: 148,466,181-148,693,393 , GRCh37.p13 chrX|NW_004070890.2: 4,909,048-5,136,108 EOLA1-DT, IDS, 8 more genes
    nsv7051521inversion1nstd229human GRCh38 chrX: 149,498,517-149,809,812 , GRCh37.p13 chrX|NW_004070890.2: 5,022,915-5,334,210 , GRCh37.p13 chrX: 148,580,048-148,891,474 MAGEA9B, MAGEA7P, 15 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
    nsv7048519inversion1nstd229human GRCh38 chrX: 147,043,248-151,148,932 , GRCh37.p13 chrX|NW_004070890.2: 2,567,639-6,530,008 , GRCh37.p13 chrX: 146,124,766-150,174,083 MIR514B, IDSP1, 67 more genes
    nsv7048225inversion1nstd229human GRCh38 chrX: 149,355,877-149,689,933 , GRCh37.p13 chrX|NW_004070890.2: 4,880,274-5,214,331 , GRCh37.p13 chrX: 148,437,407-148,771,593 EOLA1, LOC107985667, 10 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
    nsv7046541inversion1nstd229human GRCh38 chrX: 147,029,278-151,057,215 , GRCh37.p13 chrX: 146,110,796-150,174,083 , GRCh37.p13 chrX|NW_004070890.2: 2,553,669-6,530,008 MAGEA9, MIR509-3, 67 more genes
    nsv7045703inversion1nstd229human GRCh38 chrX: 149,232,833-149,701,991 , GRCh37.p13 chrX|NW_004070890.2: 4,757,230-5,226,389 , GRCh37.p13 chrX: 148,314,363-148,783,651 IDSP1, IDS2, 10 more genes
    nsv7043638inversion1nstd229human GRCh38 chrX: 145,071,588-152,199,155 , GRCh37.p13 chrX|NW_004070890.2: 595,981-6,530,008 , GRCh37.p13 chrX: 144,153,108-150,174,083 AFF2, CXorf51B, 110 more genes
    nsv7039987inversion1nstd229human GRCh38 chrX: 145,076,609-150,429,513 , GRCh37.p13 chrX|NW_004070890.2: 601,002-5,953,911 , GRCh37.p13 chrX: 144,158,129-149,597,776 MIR891A, MIR508, 78 more genes
    nsv7038763inversion1nstd229human GRCh38 chrX: 149,485,123-149,719,213 , GRCh37.p13 chrX|NW_004070890.2: 5,009,521-5,243,611 , GRCh37.p13 chrX: 148,566,654-148,800,873 IDS2, HSFX3, 9 more genes
    nsv7038250inversion1nstd229human GRCh38 chrX: 149,541,502-149,997,488 , GRCh37.p13 chrX|NW_004070890.2: 5,065,900-5,521,886 , GRCh37.p13 chrX: 148,623,047-149,165,719 TMEM185A, HSFX3, 18 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