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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3105920copy number variation1estd209human GRCh37 chr7: 122,336,555-122,336,562 , GRCh38.p12 chr7: 122,696,501-122,696,508 RNF133, CADPS2
    esv3105921copy number variation1estd209human GRCh37 chr7: 122,336,569-122,336,572 , GRCh38.p12 chr7: 122,696,515-122,696,518 RNF133, CADPS2
    nsv365281copy number variation1nstd6human NCBI35 chr7: 121,930,507-121,930,518 , GRCh37.p13 chr7: 122,336,556-122,336,567 , GRCh38.p12 chr7: 122,696,502-122,696,513 RNF133, CADPS2
    nsv2525866short tandem repeat1nstd128human GRCh37 chr7: 122,336,905-122,336,927 , GRCh38.p12 chr7: 122,696,851-122,696,873 RNF133, CADPS2
    nsv3917215copy number variation1nstd102humanLikely benign NCBI36 chr7: 122,113,100-122,158,830 , GRCh37 chr7: 122,325,864-122,371,594 , GRCh38 chr7: 122,685,810-122,731,540 RNF133, RNF148, 1 more genes
    nsv3910246copy number variation1nstd102humanUncertain significance GRCh37 chr7: 122,320,419-122,412,493 , GRCh38 chr7: 122,680,365-122,772,439 , NCBI36 chr7: 122,107,655-122,199,729 RNF133, RNF148, 2 more genes
    nsv6821539copy number variation1nstd229human GRCh38 chr7: 122,692,229-122,700,578 , GRCh37.p13 chr7: 122,332,283-122,340,632 RNF133, RNF148, 1 more genes
    nsv6631824copy number variation1nstd224human GRCh37 chr7: 122,307,692-122,427,731 , GRCh38.p12 chr7: 122,667,638-122,787,677 RNF133, RNF148, 2 more genes
    nsv6631758copy number variation1nstd224human GRCh37 chr7: 122,286,939-122,392,897 , GRCh38.p12 chr7: 122,646,885-122,752,843 RNF133, RNF148, 2 more genes
    nsv3119397copy number variation2nstd151human GRCh37 chr7: 122,337,839-122,342,807 , GRCh38.p12 chr7: 122,697,785-122,702,753 RNF133, CADPS2, 1 more genes
    nsv1191295copy number variation1nstd113human NCBI36 chr7: 121,745,810-122,125,859 , GRCh37.p13 chr7: 121,958,574-122,338,623 , GRCh38.p12 chr7: 122,318,520-122,698,569 RNF133, CADPS2, 2 more genes
    nsv1017029copy number variation1nstd100human NCBI36 chr7: 121,745,810-122,125,859 , GRCh37.p13 chr7: 121,958,574-122,338,623 , GRCh38.p12 chr7: 122,318,520-122,698,569 RNF133, RPS26P31, 2 more genes
    esv3775133copy number variation1estd192human GRCh37 chr7: 122,253,644-122,486,594 , GRCh38.p12 chr7: 122,613,590-122,846,540 RNF133, RPS26P31, 2 more genes
    esv3767748copy number variation1estd192human GRCh37 chr7: 122,338,583-122,339,796 , GRCh38.p12 chr7: 122,698,529-122,699,742 RNF133, CADPS2, 1 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNF133, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 RNF133, LOC107986817, 2014 more genes
    nsv3916726copy number variation1nstd102humanPathogenic NCBI36 chr7: 116,754,095-134,125,980 , GRCh38 chr7: 117,326,805-134,790,689 , GRCh37 chr7: 116,966,859-134,475,440 RNF133, LOC107986845, 245 more genes
    nsv4675322copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860 RNF133, CBLL1-AS1, 168 more genes
    nsv3900620copy number variation1nstd102humanPathogenic GRCh37 chr7: 111,613,396-127,897,316 , GRCh38.p12 chr7: 111,973,341-128,257,263 RNF133, LSM8, 170 more genes
    nsv3923570copy number variation1nstd102humanPathogenic NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527 RNF133, ANKRD7, 142 more genes
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