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 303

    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
    nsv7084927copy number variation1nstd229human GRCh38 chrX: 145,965,780-146,009,275 , GRCh37.p13 chrX: 145,047,298-145,090,793 , GRCh37.p13 chrX|NW_004070890.2: 1,490,171-1,533,666 MIR888, MIR890, 4 more genes
    nsv7084925copy number variation1nstd229human GRCh38 chrX: 145,962,173-146,202,683 , GRCh37.p13 chrX: 145,043,691-145,284,201 , GRCh37.p13 chrX|NW_004070890.2: 1,486,564-1,727,074 MIR891A, MIR891B, 5 more genes
    nsv7084924copy number variation1nstd229human GRCh37.p13 chrX|NW_004070890.2: 1,473,250-1,554,120 , GRCh38 chrX: 145,948,859-146,029,729 , GRCh37.p13 chrX: 145,030,377-145,111,247 MIR891A, MIR891B, 5 more genes
    nsv7084916copy number variation1nstd229human GRCh37.p13 chrX|NW_004070890.2: 1,425,792-1,585,791 , GRCh38 chrX: 145,901,401-146,061,400 , GRCh37.p13 chrX: 144,982,919-145,142,918 MIR891B, MIR892B, 5 more genes
    nsv7084909copy number variation1nstd229human GRCh37.p13 chrX|NW_004070890.2: 1,404,523-1,535,903 , GRCh38 chrX: 145,880,132-146,011,512 , GRCh37.p13 chrX: 144,961,650-145,093,030 MIR891B, MIR892B, 4 more genes
    nsv7084904copy number variation1nstd229human GRCh38 chrX: 145,849,877-146,630,749 , GRCh37.p13 chrX|NW_004070890.2: 1,374,268-2,155,140 , GRCh37.p13 chrX: 144,931,395-145,712,267 MIR891B, MIR891A, 10 more genes
    nsv7084903copy number variation1nstd229human GRCh38 chrX: 145,834,040-146,165,624 , GRCh37.p13 chrX: 144,915,558-145,247,142 , GRCh37.p13 chrX|NW_004070890.2: 1,358,431-1,690,015 MIR888, MIR892C, 6 more genes
    nsv7084891copy number variation1nstd229human GRCh38 chrX: 145,713,739-145,999,892 , GRCh37.p13 chrX: 144,795,257-145,081,410 , GRCh37.p13 chrX|NW_004070890.2: 1,238,130-1,524,283 UFM1P1, MIR892C, 7 more genes
    nsv7053159inversion1nstd229human GRCh38 chrX: 143,356,368-146,168,320 , GRCh37.p13 chrX|NW_004070890.2: 1-1,692,711 , GRCh37.p13 chrX: 142,444,161-145,249,838 MIR888, MIR890, 22 more genes
    nsv7052188inversion1nstd229human GRCh38 chrX: 143,871,359-146,052,824 , GRCh37.p13 chrX|NW_004070890.2: 1-1,577,215 , GRCh37.p13 chrX: 142,954,450-145,134,342 MIR890, MIR888, 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
    nsv7050125inversion1nstd229human GRCh38 chrX: 144,787,062-147,271,837 , GRCh37.p13 chrX|NW_004070890.2: 311,456-2,796,228 , GRCh37.p13 chrX: 143,868,583-146,353,355 MIR891B, MIR892B, 34 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
    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
    nsv6637060copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,510,129-145,119,351 , GRCh38.p12 chrX: 140,427,964-146,037,833 LOC101928833, MIR891A, 55 more genes
    nsv6637054copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,493,806-148,855,992 , GRCh38.p12 chrX: 140,411,641-149,774,334 SPANXN4, RRM2P4, 109 more genes
    nsv6636431copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,504,564-149,382,013 , GRCh38.p12 chrX: 140,422,399-150,213,783 MTND1P33, MIR514A1, 119 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center