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Items: 1 to 20 of 318

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137165copy number variation1nstd102humanUncertain significance GRCh37 chrX: 151,999,510-152,037,908 , GRCh38.p12 chrX: 152,830,966-152,869,364 NSDHL, CETN2
    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
    nsv7079666copy number variation1nstd229human GRCh38 chrX: 152,810,766-152,936,044 , GRCh37.p13 chrX|NW_003871103.3: 244,749-370,027 , GRCh37.p13 chrX: 151,979,298-152,104,588 ZNF185, CETN2, 2 more genes
    nsv7079665copy number variation1nstd229human GRCh38 chrX: 152,806,762-152,869,714 , GRCh37.p13 chrX|NW_003871103.3: 240,745-303,697 , GRCh37.p13 chrX: 151,975,296-152,038,258 NSDHL, CETN2
    nsv7079661copy number variation1nstd229human GRCh38 chrX: 152,743,133-152,950,602 , GRCh37.p13 chrX|NW_003871103.3: 177,116-384,585 , GRCh37.p13 chrX: 151,958,440-152,119,146 MAGEA2, ZNF185, 7 more genes
    nsv7079660copy number variation1nstd229human GRCh38 chrX: 152,743,001-152,869,400 , GRCh37.p13 chrX|NW_003871103.3: 176,984-303,383 , GRCh37.p13 chrX: 151,958,440-152,037,944 MAGEA6, PSMAGEA, 5 more genes
    nsv7079659copy number variation1nstd229human GRCh38 chrX: 152,739,411-152,907,344 , GRCh37.p13 chrX|NW_003871103.3: 173,394-341,327 , GRCh37.p13 chrX: 151,958,440-152,075,888 MAGEA2, ZNF185, 7 more genes
    nsv7079657copy number variation1nstd229human GRCh38 chrX: 152,735,842-152,928,396 , GRCh37.p13 chrX: 151,958,440-152,096,940 , GRCh37.p13 chrX|NW_003871103.3: 169,825-362,379 NSDHL, CSAG3, 9 more genes
    nsv7079655copy number variation1nstd229human GRCh38 chrX: 152,665,874-152,960,330 , GRCh37.p13 chrX|NW_003871103.3: 99,857-394,313 , GRCh37.p13 chrX: 151,834,345-152,128,874 MAGEA3, LOC105373372, 15 more genes
    nsv7057928inversion1nstd229human GRCh38 chrX: 152,528,769-155,098,506 , GRCh37.p13 chrX: 151,734,490-154,326,781 , GRCh37.p13 chrX|NW_003871103.3: 1-2,532,485 F8, ATP6AP1, 128 more genes
    nsv7055777inversion1nstd229human GRCh38 chrX: 152,815,342-152,858,797 , GRCh37.p13 chrX|NW_003871103.3: 249,325-292,780 , GRCh37.p13 chrX: 151,983,874-152,027,341 NSDHL, CETN2
    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
    nsv7050106inversion1nstd229human GRCh38 chrX: 152,727,074-152,847,313 , GRCh37.p13 chrX|NW_003871103.3: 161,057-281,296 , GRCh37.p13 chrX: 151,847,041-151,909,928 MAGEA2, CETN2, 8 more genes
    nsv7047350inversion1nstd229human GRCh38 chrX: 152,804,727-153,017,156 , GRCh37.p13 chrX|NW_003871103.3: 238,710-451,139 , GRCh37.p13 chrX: 151,973,263-152,185,700 PNMA5, LOC105373372, 3 more genes
    nsv7046320inversion1nstd229human GRCh38 chrX: 152,800,888-155,032,704 , GRCh37.p13 chrX|NW_003871103.3: 234,871-2,466,683 , GRCh37.p13 chrX: 151,969,427-154,260,979 FUNDC2, PNCK, 111 more genes
    nsv7046188inversion1nstd229human GRCh38 chrX: 152,545,731-155,311,806 , GRCh37.p13 chrX: 151,734,490-154,541,118 , GRCh37.p13 chrX|NW_003871103.3: 1-2,745,785 TEX28, SSR4, 133 more genes
    nsv7041676inversion1nstd229human GRCh38 chrX: 152,678,626-152,860,413 , GRCh37.p13 chrX|NW_003871103.3: 112,609-294,396 , GRCh37.p13 chrX: 151,847,041-151,958,394 CSAG3, NSDHL, 13 more genes
    nsv7038456inversion1nstd229human GRCh38 chrX: 152,791,429-152,850,808 , GRCh37.p13 chrX: 151,959,973-152,019,352 , GRCh37.p13 chrX|NW_003871103.3: 225,412-284,791 NSDHL, MAGEA6-DT, 1 more genes
    nsv6636982copy number variation1nstd102humanUncertain significance GRCh37 chrX: 151,869,765-152,101,001 , GRCh38.p12 chrX: 152,701,287-152,932,457 CETN2, CSAG4, 13 more genes
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