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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054299inversion1nstd229human GRCh38 chr7: 114,723,718-115,439,356 , GRCh37.p13 chr7: 114,363,773-115,079,410 RAC1P6, MDFIC, 2 more genes
    nsv7053581inversion1nstd229human GRCh38 chr7: 114,893,355-115,139,860 , GRCh37.p13 chr7: 114,533,410-114,779,914 MDFIC, RAC1P6, 2 more genes
    nsv6837761copy number variation1nstd229human GRCh38 chr7: 115,030,401-115,167,400 , GRCh37.p13 chr7: 114,670,455-114,807,454 RAC1P6, LINC01392, 1 more genes
    nsv6836774copy number variation1nstd229human GRCh38 chr7: 115,117,414-115,117,519 , GRCh37.p13 chr7: 114,757,468-114,757,573 LINC01393
    nsv6835204copy number variation1nstd229human GRCh38 chr7: 115,090,958-115,091,579 , GRCh37.p13 chr7: 114,731,012-114,731,633 LINC01393
    nsv6832207copy number variation1nstd229human GRCh38 chr7: 115,090,537-115,094,164 , GRCh37.p13 chr7: 114,730,591-114,734,218 LINC01393
    nsv6831475copy number variation1nstd229human GRCh38 chr7: 110,527,230-117,297,230 , GRCh37.p13 chr7: 110,167,287-116,937,284 IMMP2L, LOC105375466, 66 more genes
    nsv6830342copy number variation1nstd229human GRCh38 chr7: 115,122,257-115,153,376 , GRCh37.p13 chr7: 114,762,311-114,793,430 LINC01393, LINC01392, 1 more genes
    nsv6829714copy number variation1nstd229human GRCh38 chr7: 115,031,101-115,416,600 , GRCh37.p13 chr7: 114,671,155-115,056,654 RAC1P6, LINC01392, 1 more genes
    nsv6829546copy number variation1nstd229human GRCh38 chr7: 115,076,184-115,091,942 , GRCh37.p13 chr7: 114,716,238-114,731,996 LINC01393
    nsv6828346copy number variation1nstd229human GRCh38 chr7: 115,030,201-115,168,100 , GRCh37.p13 chr7: 114,670,255-114,808,154 LINC01393, LINC01392, 1 more genes
    nsv6827706copy number variation1nstd229human GRCh38 chr7: 115,001,201-115,123,700 , GRCh37.p13 chr7: 114,641,255-114,763,754 LINC01392, LINC01393, 1 more genes
    nsv6826849copy number variation1nstd229human GRCh38 chr7: 115,029,401-115,167,800 , GRCh37.p13 chr7: 114,669,455-114,807,854 LINC01393, LINC01392, 1 more genes
    nsv6826783copy number variation1nstd229human GRCh38 chr7: 115,061,442-115,291,080 , GRCh37.p13 chr7: 114,701,496-114,931,134 LINC01392, LINC01393, 1 more genes
    nsv6825667copy number variation1nstd229human GRCh38 chr7: 115,087,706-115,095,072 , GRCh37.p13 chr7: 114,727,760-114,735,126 LINC01393
    nsv6823123copy number variation1nstd229human GRCh38 chr7: 115,029,201-115,147,300 , GRCh37.p13 chr7: 114,669,255-114,787,354 LINC01393, LINC01392, 1 more genes
    nsv6820698copy number variation1nstd229human GRCh38 chr7: 115,075,299-115,080,954 , GRCh37.p13 chr7: 114,715,353-114,721,008 LINC01393
    nsv6820439copy number variation1nstd229human GRCh38 chr7: 115,119,526-115,138,645 , GRCh37.p13 chr7: 114,759,580-114,778,699 LINC01392, LINC01393, 1 more genes
    nsv6819662copy number variation1nstd229human GRCh38 chr7: 115,096,934-115,118,377 , GRCh37.p13 chr7: 114,736,988-114,758,431 LINC01393
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
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