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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148084copy number variation1nstd102humanPathogenic GRCh37 chr3: 3,669,542-9,937,745 , GRCh38.p12 chr3: 3,627,858-9,896,061 LOC105376943, GRM7-AS2, 71 more genes
    nsv7055847inversion1nstd229human GRCh38 chr3: 5,111,802-11,290,661 , GRCh37.p13 chr3: 5,153,487-11,332,347 GHRLOS, LHFPL4, 96 more genes
    nsv7049987inversion1nstd229human GRCh38 chr3: 4,474,487-6,085,126 , GRCh37.p13 chr3: 4,516,171-6,126,813 LOC105376940, RNF10P1, 18 more genes
    nsv7049678inversion1nstd229human GRCh38 chr3: 1,801,851-5,900,150 , GRCh37.p13 chr3: 1,843,535-5,941,837 ITPR1, SUMF1, 34 more genes
    nsv7042276inversion1nstd229human GRCh38 chr3: 5,046,528-5,705,640 , GRCh37.p13 chr3: 5,088,213-5,747,327 MRPS35P1, LOC105376938, 8 more genes
    nsv6718032copy number variation1nstd229human GRCh38 chr3: 4,790,507-6,492,604 , GRCh37.p13 chr3: 4,832,191-6,534,291 UBTFL8, LOC105376936, 15 more genes
    nsv6717901copy number variation1nstd229human GRCh38 chr3: 5,203,171-5,203,272 , GRCh37.p13 chr3: 5,244,856-5,244,957 EDEM1
    nsv6717058copy number variation1nstd229human GRCh38 chr3: 5,193,041-5,207,073 , GRCh37.p13 chr3: 5,234,726-5,248,758 EDEM1
    nsv6716148copy number variation1nstd229human GRCh38 chr3: 5,174,512-5,344,848 , GRCh37.p13 chr3: 5,216,197-5,386,533 ARL8B, EDEM1, 2 more genes
    nsv6714151copy number variation1nstd229human GRCh38 chr3: 5,200,201-5,422,100 , GRCh37.p13 chr3: 5,241,886-5,463,786 RN7SL553P, MIR4790, 1 more genes
    nsv6713757copy number variation1nstd229human GRCh38 chr3: 5,199,757-5,207,833 , GRCh37.p13 chr3: 5,241,442-5,249,518 EDEM1
    nsv6710780copy number variation1nstd229human GRCh38 chr3: 5,086,840-6,025,909 , GRCh37.p13 chr3: 5,128,525-6,067,596 LOC102723596, ARL8B, 9 more genes
    nsv6709602copy number variation1nstd229human GRCh38 chr3: 4,173,620-5,491,643 , GRCh37.p13 chr3: 4,215,304-5,533,330 BHLHE40-AS1, SETMAR, 15 more genes
    nsv6709538copy number variation1nstd229human GRCh38 chr3: 4,892,087-5,367,763 , GRCh37.p13 chr3: 4,933,771-5,409,448 BHLHE40-AS1, RNF10P1, 6 more genes
    nsv6709260copy number variation1nstd229human GRCh38 chr3: 5,043,605-5,209,418 , GRCh37.p13 chr3: 5,085,290-5,251,103 RNF10P1, ARL8B, 2 more genes
    nsv6706686copy number variation1nstd229human GRCh38 chr3: 5,189,227-5,192,916 , GRCh37.p13 chr3: 5,230,912-5,234,601 EDEM1
    nsv6704397copy number variation1nstd229human GRCh38 chr3: 5,190,955-5,350,986 , GRCh37.p13 chr3: 5,232,640-5,392,671 RN7SL553P, EDEM1, 1 more genes
    nsv6704357copy number variation1nstd229human GRCh38 chr3: 5,062,401-5,251,800 , GRCh37.p13 chr3: 5,104,086-5,293,485 RN7SL553P, ARL8B, 4 more genes
    nsv6704317copy number variation1nstd229human GRCh38 chr3: 2,434,186-5,652,877 , GRCh37.p13 chr3: 2,475,870-5,694,564 IL5RA, RNF10P1, 26 more genes
    nsv6701032copy number variation1nstd229human GRCh38 chr3: 5,204,545-5,213,798 , GRCh37.p13 chr3: 5,246,230-5,255,483 EDEM1
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