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Items: 1 to 20 of 849

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098482copy number variation1nstd102humanPathogenic GRCh37 chrX: 10,491,112-10,535,587 , GRCh38.p12 chrX: 10,523,072-10,567,547 MID1
    nsv7098208copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chrX: 10,450,500-10,450,688 , GRCh38.p12 chrX: 10,482,460-10,482,648 MID1
    nsv7098207copy number variation1nstd102humanPathogenic GRCh37 chrX: 10,417,408-10,423,137 , GRCh38.p12 chrX: 10,449,368-10,455,097 MID1
    nsv7078063copy number variation1nstd229human GRCh38 chrX: 10,539,607-10,542,657 , GRCh37.p13 chrX: 10,507,647-10,510,697 MID1
    nsv7078031copy number variation1nstd229human GRCh38 chrX: 10,660,283-10,660,500 , GRCh37.p13 chrX: 10,628,323-10,628,540 MID1
    nsv7077976copy number variation1nstd229human GRCh38 chrX: 10,428,917-11,410,756 , GRCh37.p13 chrX: 10,396,957-11,428,876 ARHGAP6, GOT2P7, 5 more genes
    nsv7077221copy number variation1nstd229human GRCh38 chrX: 10,577,325-11,333,209 , GRCh37.p13 chrX: 10,545,365-11,351,329 ARHGAP6, GOT2P7, 5 more genes
    nsv7076553copy number variation1nstd229human GRCh38 chrX: 10,709,209-10,727,685 , GRCh37.p13 chrX: 10,677,249-10,695,725 MID1
    nsv7076493copy number variation1nstd229human GRCh38 chrX: 10,587,038-10,587,761 , GRCh37.p13 chrX: 10,555,078-10,555,801 MID1
    nsv7076203copy number variation1nstd229human GRCh38 chrX: 10,525,201-10,551,000 , GRCh37.p13 chrX: 10,493,241-10,519,040 MID1
    nsv7076152copy number variation1nstd229human GRCh38 chrX: 10,642,301-10,642,800 , GRCh37.p13 chrX: 10,610,341-10,610,840 MID1
    nsv7076120copy number variation1nstd229human GRCh38 chrX: 10,648,920-10,652,308 , GRCh37.p13 chrX: 10,616,960-10,620,348 MID1
    nsv7075971copy number variation1nstd229human GRCh38 chrX: 10,458,677-10,459,027 , GRCh37.p13 chrX: 10,426,717-10,427,067 MID1
    nsv7075657copy number variation1nstd229human GRCh38 chrX: 10,833,804-10,839,581 , GRCh37.p13 chrX: 10,851,923-10,857,700 MID1
    nsv7075357copy number variation1nstd229human GRCh38 chrX: 10,677,898-10,685,148 , GRCh37.p13 chrX: 10,645,938-10,653,188 MID1
    nsv7075225copy number variation1nstd229human GRCh38 chrX: 10,513,530-10,513,709 , GRCh37.p13 chrX: 10,481,570-10,481,749 MID1
    nsv7074764copy number variation1nstd229human GRCh38 chrX: 10,824,972-10,829,003 , GRCh37.p13 chrX: 10,843,091-10,847,122 MID1
    nsv7074612copy number variation1nstd229human GRCh38 chrX: 10,825,545-10,852,131 , GRCh37.p13 chrX: 10,843,664-10,870,250 MID1
    nsv7074245copy number variation1nstd229human GRCh38 chrX: 10,151,101-10,603,800 , GRCh37.p13 chrX: 10,119,141-10,571,840 CLCN4, MID1, 1 more genes
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