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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
    nsv7098108copy number variation1nstd102humanUncertain significance GRCh37 chrX: 106,456,106-106,959,200 , GRCh38.p12 chrX: 107,212,876-107,715,970 TSC22D3, DNAAF6, 6 more genes
    nsv7098107copy number variation1nstd102humanPathogenic GRCh37 chrX: 106,046,084-108,868,249 , GRCh38.p12 chrX: 106,802,854-109,625,020 VSIG1, NXT2, 32 more genes
    nsv7078305copy number variation1nstd229human GRCh38 chrX: 107,605,046-107,697,234 , GRCh37.p13 chrX: 106,848,276-106,940,464 PRPS1, FRMPD3
    nsv7078304copy number variation1nstd229human GRCh38 chrX: 107,601,482-107,601,522 , GRCh37.p13 chrX: 106,844,712-106,844,752 FRMPD3
    nsv7078303copy number variation1nstd229human GRCh38 chrX: 107,591,094-107,604,500 , GRCh37.p13 chrX: 106,834,324-106,847,730 FRMPD3
    nsv7078302copy number variation1nstd229human GRCh38 chrX: 107,590,701-107,613,800 , GRCh37.p13 chrX: 106,833,931-106,857,030 FRMPD3
    nsv7078301copy number variation1nstd229human GRCh38 chrX: 107,589,876-107,593,166 , GRCh37.p13 chrX: 106,833,106-106,836,396 FRMPD3
    nsv7078300copy number variation1nstd229human GRCh38 chrX: 107,582,101-107,604,800 , GRCh37.p13 chrX: 106,825,331-106,848,030 FRMPD3
    nsv7078299copy number variation1nstd229human GRCh38 chrX: 107,571,422-107,571,941 , GRCh37.p13 chrX: 106,814,652-106,815,171 FRMPD3
    nsv7078298copy number variation1nstd229human GRCh38 chrX: 107,567,887-107,568,092 , GRCh37.p13 chrX: 106,811,117-106,811,322 FRMPD3
    nsv7078297copy number variation1nstd229human GRCh38 chrX: 107,552,701-107,555,600 , GRCh37.p13 chrX: 106,795,931-106,798,830 FRMPD3
    nsv7078296copy number variation1nstd229human GRCh38 chrX: 107,546,282-107,572,743 , GRCh37.p13 chrX: 106,789,512-106,815,973 FRMPD3-AS1, FRMPD3
    nsv7078295copy number variation1nstd229human GRCh38 chrX: 107,533,457-107,533,646 , GRCh37.p13 chrX: 106,776,687-106,776,876 FRMPD3, FRMPD3-AS1
    nsv7078294copy number variation1nstd229human GRCh38 chrX: 107,526,826-107,538,725 , GRCh37.p13 chrX: 106,770,056-106,781,955 FRMPD3, FRMPD3-AS1
    nsv7078293copy number variation1nstd229human GRCh38 chrX: 107,516,266-107,527,887 , GRCh37.p13 chrX: 106,759,496-106,771,117 FRMPD3-AS1, FRMPD3
    nsv7078292copy number variation1nstd229human GRCh38 chrX: 107,512,168-107,521,442 , GRCh37.p13 chrX: 106,755,398-106,764,672 FRMPD3, FRMPD3-AS1
    nsv7078290copy number variation1nstd229human GRCh38 chrX: 107,496,201-107,552,000 , GRCh37.p13 chrX: 106,739,431-106,795,230 FRMPD3, FRMPD3-AS1
    nsv7078262copy number variation1nstd229human GRCh38 chrX: 107,064,984-107,532,736 , GRCh37.p13 chrX: 106,308,214-106,775,966 FRMPD3-AS1, FRMPD3, 7 more genes
    nsv7052621inversion1nstd229human GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650 CSGALNACT2P2, LOC107985662, 82 more genes
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