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Items: 1 to 20 of 296

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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
    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
    nsv7079616copy number variation1nstd229human GRCh38 chrX: 152,264,528-152,792,675 , GRCh37.p13 chrX: 151,433,000-151,734,489 CSAG2, MAGEA2, 17 more genes
    nsv7057941inversion1nstd229human GRCh38 chrX: 152,675,413-152,794,779 , GRCh37.p13 chrX|NW_003871103.3: 109,396-228,762 MAGEA3, MAGEA6, 11 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
    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
    nsv7048245inversion1nstd229human GRCh38 chrX: 152,742,942-152,790,105 , GRCh37.p13 chrX: 151,847,041-151,894,019 , GRCh37.p13 chrX|NW_003871103.3: 176,925-224,088 MAGEA2, PSMAGEA, 3 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
    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
    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
    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
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