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Items: 1 to 20 of 293

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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
    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
    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
    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
    nsv6633793copy number variation1nstd224human GRCh37 chrX: 151,429,728-151,910,051 , GRCh38.p12 chrX: 152,261,256-152,729,753 GABRA3, CSAG1, 10 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
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
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