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Items: 1 to 20 of 339

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    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
    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
    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
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