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Items: 1 to 20 of 187

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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
    nsv7096474copy number variation1nstd102humanPathogenic GRCh37 chr3: 6,903,076-9,517,775 , GRCh38.p12 chr3: 6,861,389-9,476,091 SRGAP3-AS2, SRGAP3-AS3, 23 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
    nsv7053391inversion1nstd229human GRCh38 chr3: 9,368,610-9,370,162 , GRCh37.p13 chr3: 9,410,294-9,411,846 THUMPD3
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv7042733inversion1nstd229human GRCh38 chr3: 9,176,576-9,386,566 , GRCh37.p13 chr3: 9,218,260-9,428,250 SRGAP3, SRGAP3-AS4, 5 more genes
    nsv6715267copy number variation1nstd229human GRCh38 chr3: 9,052,999-9,369,738 , GRCh37.p13 chr3: 9,094,683-9,411,422 SRGAP3-AS2, PGAM1P4, 4 more genes
    nsv6706690copy number variation1nstd229human GRCh38 chr3: 9,368,167-9,378,962 , GRCh37.p13 chr3: 9,409,851-9,420,646 THUMPD3
    nsv6706387copy number variation1nstd229human GRCh38 chr3: 9,368,724-9,385,500 , GRCh37.p13 chr3: 9,410,408-9,427,184 THUMPD3, THUMPD3-AS1
    nsv6705356copy number variation1nstd229human GRCh38 chr3: 9,260,412-9,373,147 , GRCh37.p13 chr3: 9,302,096-9,414,831 THUMPD3, PGAM1P4, 1 more genes
    nsv6701916copy number variation1nstd229human GRCh38 chr3: 9,374,783-9,375,458 , GRCh37.p13 chr3: 9,416,467-9,417,142 THUMPD3
    nsv6698658copy number variation1nstd229human GRCh38 chr3: 9,366,836-9,367,017 , GRCh37.p13 chr3: 9,408,520-9,408,701 THUMPD3
    nsv6637145copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,931-10,687,964 , GRCh38.p12 chr3: 19,253-10,646,279 RN7SL120P, LOC105376940, 132 more genes
    nsv6636427copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,113,024-9,477,562 , GRCh38.p12 chr3: 9,071,340-9,435,878 SRGAP3-AS4, THUMPD3-AS1, 6 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
    nsv6546782inversion1nstd223human GRCh38 chr3: 9,368,610-9,370,162 , GRCh37.p13 chr3: 9,410,294-9,411,846 THUMPD3
    nsv6540919inversion1nstd223human GRCh38 chr3: 9,115,607-13,898,149 , GRCh37.p13 chr3: 9,157,291-13,939,646 MKRN2OS, RAF1, 106 more genes
    nsv6372949copy number variation1nstd223human GRCh38 chr3: 9,260,411-9,373,146 , GRCh37.p13 chr3: 9,302,095-9,414,830 THUMPD3, SRGAP3, 1 more genes
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