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Items: 1 to 20 of 197

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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
    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
    nsv7047870inversion1nstd229human GRCh38 chr3: 3,384,572-5,027,295 , GRCh37.p13 chr3: 3,426,256-5,068,980 ITPR1-DT, BHLHE40, 11 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
    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
    nsv6713223copy number variation1nstd229human GRCh38 chr3: 4,980,409-4,982,835 , GRCh37.p13 chr3: 5,022,094-5,024,520 BHLHE40, BHLHE40-AS1
    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
    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
    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
    nsv6636788copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 3,718,732-5,377,364 , GRCh38.p12 chr3: 3,677,048-5,335,679 ITPR1, SETMAR, 17 more genes
    nsv6636323copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-9,769,457 , GRCh38.p12 chr3: 20,214-9,727,773 LOC107984112, LRRN1, 92 more genes
    nsv6636296copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-9,899,605 , GRCh38.p12 chr3: 20,214-9,857,921 GRM7-AS1, LOC105376938, 101 more genes
    nsv6636276copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035 RPL23AP39, LOC107986059, 144 more genes
    nsv6373355copy number variation1nstd223human GRCh38 chr3: 3,629,462-6,680,981 , GRCh37.p13 chr3: 3,671,146-6,722,668 BHLHE40, MRPS10P2, 26 more genes
    nsv6313662copy number variation1nstd102humanUncertain significance GRCh37 chr3: 4,876,684-7,615,554 , GRCh38.p12 chr3: 4,835,000-7,573,867 MRPS36P1, GRM7, 23 more genes
    nsv6313525copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-9,797,094 , GRCh38.p12 chr3: 20,213-9,755,410 EGOT, LOC107986040, 95 more genes
    nsv6135015copy number variation1nstd213human GRCh37 chr3: 4,730,000-5,230,001 , GRCh38.p12 chr3: 4,688,316-5,188,316 ITPR1, BHLHE40, 6 more genes
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