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Items: 1 to 20 of 333

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137678copy number variation1nstd102humanPathogenic GRCh37 chrX: 148,585,691-148,585,775 , GRCh38 chrX: 149,504,161-149,504,245 IDS
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv6112666copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,484,271-149,442,579 , GRCh38.p12 chrX: 140,402,106-150,274,366 MIR508, SPANXN1, 121 more genes
    nsv5974046inversion1nstd209human GRCh37.p13 chrX: 148,570,390-148,608,105 , GRCh38 chrX: 149,488,859-149,526,566 , GRCh37.p13 chrX|NW_004070890.2: 5,013,257-5,050,964 IDS, IDSP1, 2 more genes
    nsv5673907copy number variation1nstd102humanPathogenic GRCh37 chrX: 148,571,835-148,582,578 , GRCh38.p12 chrX: 149,490,304-149,501,047 IDS
    nsv5607497insertion1nstd207human GRCh38 chrX: 149,490,732-149,490,732 , GRCh37.p13 chrX|NW_004070890.2: 5,015,130-5,015,130 , GRCh37.p13 chrX: 148,572,263-148,572,263 IDS
    nsv5563162inversion1nstd206human GRCh37.p13 chrX|NW_004070890.2: 5,011,888-5,052,365 , GRCh38 chrX: 149,487,490-149,527,967 , GRCh37.p13 chrX: 148,569,021-148,609,506 IDS, IDSP1, 2 more genes
    nsv5547173insertion1nstd206human GRCh38 chrX: 149,490,724-149,490,724 , GRCh37.p13 chrX|NW_004070890.2: 5,015,122-5,015,122 , GRCh37.p13 chrX: 148,572,255-148,572,255 IDS
    nsv5429574copy number variation1nstd206human GRCh37.p13 chrX|NW_004070890.2: 5,023,398-5,116,004 , GRCh38 chrX: 149,499,000-149,591,606 , GRCh37.p13 chrX: 148,580,531-148,673,270 IDS, IDSP1, 6 more genes
    nsv5427530copy number variation1nstd206human GRCh38 chrX: 149,202,856-149,768,033 , GRCh37.p13 chrX: 148,284,386-148,849,694 , GRCh37.p13 chrX|NW_004070890.2: 4,727,253-5,292,431 LOC100420322, IDS2, 13 more genes
    nsv5424778copy number variation1nstd206human GRCh38 chrX: 149,499,121-149,694,032 , GRCh37.p13 chrX|NW_004070890.2: 5,023,519-5,218,430 , GRCh37.p13 chrX: 148,580,652-148,775,692 HSFX3, IDS2, 9 more genes
    nsv5381665copy number variation1nstd102humanUncertain significance GRCh37 chrX: 148,579,628-148,579,848 , GRCh38.p12 chrX: 149,498,097-149,498,317 IDS
    nsv5377254translocation1nstd200human GRCh38 chrX: 149,691,390-149,691,390 , GRCh38 chrX: 149,492,267-149,492,267 , GRCh37.p13 chrX: 148,573,798-148,573,798 , GRCh37.p13 chrX|NW_004070890.2: 5,016,665-5,016,665 , GRCh37.p13 chrX|NW_004070890.2: 5,215,788-5,215,788 , GRCh37.p13 chrX: 148,773,050-148,773,050 IDS, MAGEA11
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv4909263copy number variation1nstd200human GRCh38 chrX: 149,308,877-149,707,503 , GRCh37.p13 chrX|NW_004070890.2: 4,833,274-5,231,901 , GRCh37.p13 chrX: 148,390,407-148,789,163 EOLA1, LOC107985667, 10 more genes
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4728473copy number variation1nstd102humanLikely benign GRCh37 chrX: 148,448,248-148,855,992 , GRCh38.p12 chrX: 149,366,718-149,774,334 MAGEA11, TMEM185A, 14 more genes
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