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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
    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
    nsv7098232copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 149,613,783-150,573,536 , GRCh38.p12 chrX: 150,445,517-151,405,064 MTM1, GPR50, 14 more genes
    nsv7091214copy number variation1nstd229human GRCh38 chrX: 150,983,432-150,983,454 , GRCh37.p13 chrX|NW_004070890.2: 6,507,830-6,507,852 , GRCh37.p13 chrX: 150,151,905-150,151,927 HMGB3
    nsv7091201copy number variation1nstd229human GRCh38 chrX: 150,886,601-150,983,700 , GRCh37.p13 chrX: 150,055,074-150,152,173 , GRCh37.p13 chrX|NW_004070890.2: 6,410,999-6,508,098 CD99L2, HMGB3, 1 more genes
    nsv7091171copy number variation1nstd229human GRCh38 chrX: 150,262,588-151,080,792 , GRCh37.p13 chrX: 149,430,802-150,174,083 , GRCh37.p13 chrX|NW_004070890.2: 5,786,986-6,530,008 RNA5SP525, CD99L2, 9 more genes
    nsv7091170copy number variation1nstd229human GRCh38 chrX: 150,253,215-151,011,085 , GRCh37.p13 chrX|NW_004070890.2: 5,777,613-6,530,008 , GRCh37.p13 chrX: 149,421,426-150,174,083 CYP2C64P, MAMLD1, 7 more genes
    nsv7085435copy number variation1nstd229human GRCh38 chrX: 150,227,830-151,085,680 , GRCh37.p13 chrX|NW_004070890.2: 5,752,228-6,530,008 , GRCh37.p13 chrX: 149,396,065-150,174,083 XRCC6P2, RNU6-383P, 11 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
    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
    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
    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
    nsv6634237copy number variation1nstd224human GRCh37 chrX: 149,422,813-154,913,173 , GRCh38.p12 chrX: 150,254,602-155,683,512 ABCD1, FLNA, 182 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
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