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Items: 1 to 20 of 347

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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
    nsv6717897copy number variation1nstd229human GRCh38 chr3: 5,124,074-5,136,148 , GRCh37.p13 chr3: 5,165,759-5,177,833 ARL8B
    nsv6717626copy number variation1nstd229human GRCh38 chr3: 4,978,936-5,133,462 , GRCh37.p13 chr3: 5,020,621-5,175,147 BHLHE40, UBTFL8, 3 more genes
    nsv6716311copy number variation1nstd229human GRCh38 chr3: 5,144,194-5,147,995 , GRCh37.p13 chr3: 5,185,879-5,189,680 ARL8B
    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
    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
    nsv6709503copy number variation1nstd229human GRCh38 chr3: 5,074,401-5,136,300 , GRCh37.p13 chr3: 5,116,086-5,177,985 UBTFL8, ARL8B
    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
    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
    nsv6699926copy number variation1nstd229human GRCh38 chr3: 5,153,477-5,160,529 , GRCh37.p13 chr3: 5,195,162-5,202,214 ARL8B
    nsv6637145copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,931-10,687,964 , GRCh38.p12 chr3: 19,253-10,646,279 RN7SL120P, LOC105376940, 132 more genes
    nsv6637133copy number variation1nstd102humanUncertain significance GRCh37 chr3: 2,347,813-6,381,546 , GRCh38.p12 chr3: 2,306,129-6,339,859 BHLHE40, EDEM1, 33 more genes
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