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Items: 1 to 20 of 445

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146461copy number variation1nstd232human GRCh37.p13 chrX: 152,807,507-152,807,577 , GRCh38.p12 chrX: 153,542,049-153,542,119 ATP2B3
    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
    nsv7098598copy number variation2nstd102humanUncertain significance GRCh37 chrX: 152,014,869-153,363,122 , GRCh38.p12 chrX: 152,846,325-154,097,665 AVPR2, HMGN2P48, 56 more genes
    nsv7097997copy number variation1nstd102humanUncertain significance GRCh37 chrX: 152,770,090-152,954,311 , GRCh38.p12 chrX: 153,504,632-153,688,856 RPL18AP16, DUSP9, 9 more genes
    nsv7097996copy number variation6nstd102humanPathogenic GRCh37 chrX: 152,014,869-155,171,615 , GRCh38.p12 chrX: 152,846,325-155,941,951 PHF10P1, ZNF185, 132 more genes
    nsv7097995copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 152,014,869-154,563,736 , GRCh38.p12 chrX: 152,846,325-155,334,427 RN7SL697P, CYCSP45, 118 more genes
    nsv7085522copy number variation1nstd229human GRCh38 chrX: 153,389,301-153,865,200 , GRCh37.p13 chrX: 152,654,759-153,130,655 , GRCh37.p13 chrX|NW_003871103.3: 823,284-1,299,183 PDZD4, ATP2B3, 26 more genes
    nsv7085521copy number variation1nstd229human GRCh38 chrX: 153,389,301-153,559,700 , GRCh37.p13 chrX|NW_003871103.3: 823,284-993,683 , GRCh37.p13 chrX: 152,654,759-152,825,158 HAUS7, RN7SL667P, 7 more genes
    nsv7085520copy number variation1nstd229human GRCh38 chrX: 153,389,201-154,074,000 , GRCh37.p13 chrX: 152,654,659-153,339,451 , GRCh37.p13 chrX|NW_003871103.3: 823,184-1,507,979 SLC6A8, PNCK, 39 more genes
    nsv7085519copy number variation1nstd229human GRCh38 chrX: 153,388,501-154,018,300 , GRCh37.p13 chrX|NW_003871103.3: 822,484-1,452,279 , GRCh37.p13 chrX: 152,653,959-153,283,751 RENBP, NAA10, 38 more genes
    nsv7085518copy number variation1nstd229human GRCh38 chrX: 153,388,501-153,588,500 , GRCh37.p13 chrX|NW_003871103.3: 822,484-1,022,483 , GRCh37.p13 chrX: 152,653,959-152,853,958 BGN, ECMXP, 8 more genes
    nsv7085517copy number variation1nstd229human GRCh38 chrX: 153,388,101-153,642,400 , GRCh37.p13 chrX|NW_003871103.3: 822,084-1,076,382 , GRCh37.p13 chrX: 152,653,559-152,907,854 PNMA6E, ATP2B3, 12 more genes
    nsv7085516copy number variation1nstd229human GRCh38 chrX: 153,386,101-153,903,500 , GRCh37.p13 chrX|NW_003871103.3: 820,084-1,337,482 , GRCh37.p13 chrX: 152,651,559-153,168,954 BCAP31, SRPK3, 28 more genes
    nsv7085514copy number variation1nstd229human GRCh38 chrX: 153,379,401-153,650,000 , GRCh37.p13 chrX: 152,644,859-152,915,455 , GRCh37.p13 chrX|NW_003871103.3: 813,384-1,083,983 ZFP92, LOC105373379, 12 more genes
    nsv7085512copy number variation1nstd229human GRCh38 chrX: 153,378,501-154,041,100 , GRCh37.p13 chrX|NW_003871103.3: 812,484-1,475,079 , GRCh37.p13 chrX: 152,643,959-153,306,551 MIR3202-2, MECP2, 39 more genes
    nsv7085511copy number variation1nstd229human GRCh38 chrX: 153,378,501-153,522,400 , GRCh37.p13 chrX|NW_003871103.3: 812,484-956,383 , GRCh37.p13 chrX: 152,643,959-152,787,858 ECMXP, TREX2, 7 more genes
    nsv7079776copy number variation1nstd229human GRCh38 chrX: 153,576,201-153,583,300 , GRCh37.p13 chrX: 152,841,659-152,848,758 , GRCh37.p13 chrX|NW_003871103.3: 1,010,184-1,017,283 ATP2B3
    nsv7079775copy number variation1nstd229human GRCh38 chrX: 153,568,031-153,568,103 , GRCh37.p13 chrX|NW_003871103.3: 1,002,014-1,002,086 , GRCh37.p13 chrX: 152,833,489-152,833,561 ATP2B3
    nsv7079774copy number variation1nstd229human GRCh38 chrX: 153,563,796-153,788,016 , GRCh37.p13 chrX|NW_003871103.3: 997,779-1,221,999 , GRCh37.p13 chrX: 152,829,254-153,053,471 ABCD1, PNCK, 14 more genes
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