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Items: 1 to 20 of 348

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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
    nsv7079134copy number variation1nstd229human GRCh38 chrX: 139,434,048-142,116,322 , GRCh37.p13 chrX: 138,516,207-141,204,108 LOC101928833, CDR1, 33 more genes
    nsv7079098copy number variation1nstd229human GRCh38 chrX: 139,214,744-145,647,139 , GRCh37.p13 chrX: 138,296,906-142,299,065 LOC101928833, ATP11C, 61 more genes
    nsv7079096copy number variation1nstd229human GRCh38 chrX: 139,212,792-142,672,772 , GRCh37.p13 chrX: 138,294,954-141,760,558 ATP11C, LOC105373345, 43 more genes
    nsv7079085copy number variation1nstd229human GRCh38 chrX: 139,139,041-142,300,202 , GRCh37.p13 chrX: 138,221,203-141,387,988 LINC00632, LOC100420230, 40 more genes
    nsv7057557inversion1nstd229human GRCh38 chrX: 141,115,375-141,729,413 , GRCh37.p13 chrX|NW_004070888.1: 211,178-825,216 , GRCh37.p13 chrX: 140,209,560-140,817,596 SPANXA1, SPANXD, 9 more genes
    nsv7054935inversion1nstd229human GRCh37.p13 chrX|NW_004070888.1: 21,168-359,325 , GRCh38 chrX: 140,925,365-141,263,522 , GRCh37.p13 chrX: 140,007,530-140,357,658 LDOC1, SPANXC, 5 more genes
    nsv7051018inversion1nstd229human GRCh37.p13 chrX|NW_004070888.1: 208,768-548,612 , GRCh38 chrX: 141,112,965-141,452,809 , GRCh37.p13 chrX: 140,207,150-140,540,804 RPL36AP52, RBMX2P2, 4 more genes
    nsv7050699inversion1nstd229human GRCh38 chrX: 140,927,445-141,226,808 , GRCh37.p13 chrX|NW_004070888.1: 23,248-322,611 , GRCh37.p13 chrX: 140,009,610-140,320,987 LDOC1, RPL36AP52, 2 more genes
    nsv7050440inversion1nstd229human GRCh37.p13 chrX|NW_004070888.1: 253,682-880,103 , GRCh38 chrX: 141,157,879-141,784,300 , GRCh37.p13 chrX: 140,252,077-140,872,086 SPANXA1, SPANXD, 7 more genes
    nsv7048945inversion1nstd229human GRCh38 chrX: 140,529,443-141,468,418 , GRCh37.p13 chrX|NW_004070888.1: 1-564,221 , GRCh37.p13 chrX: 139,986,363-140,556,412 CDR1, RNU6-3P, 9 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
    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
    nsv6634343copy number variation1nstd102humanUncertain significance GRCh37 chrX: 140,079,710-140,783,042 , GRCh38.p12 chrX: 140,997,545-141,694,885 RNU6-3P, RBMX2P2, 9 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634214copy number variation1nstd224human GRCh37 chrX: 140,221,672-140,747,402 , GRCh38.p12 chrX: 141,127,483-141,659,258 LDOC1, SPANXA1, 7 more genes
    nsv6634213copy number variation1nstd224human GRCh37 chrX: 140,210,323-140,559,721 , GRCh38.p12 chrX: 141,116,138-141,471,727 LDOC1, SPANXC, 4 more genes
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