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Items: 1 to 20 of 542

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144615copy number variation1nstd232human GRCh37.p13 chr17: 80,629,308-80,629,413 , GRCh38.p12 chr17: 82,671,432-82,671,537 RAB40B
    nsv7138092copy number variation1nstd232human GRCh37.p13 chr17: 80,630,130-80,630,238 , GRCh38.p12 chr17: 82,672,254-82,672,362 RAB40B
    nsv7137148copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,656,331-81,009,672 , GRCh38.p12 chr17: 82,698,455-83,051,796 ZNF750, FN3KRP, 5 more genes
    nsv7098933copy number variation1nstd102humanUncertain significance GRCh38 chr17: 82,004,063-83,087,346 , GRCh37.p13 chr17: 79,961,939-81,045,222 ZNF750, LINC01970, 37 more genes
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095424copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,332,201-80,758,892 , GRCh38.p12 chr17: 82,374,325-82,801,016 CYBC1, TRX-CAT1-8, 15 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7069998inversion1nstd229human GRCh38 chr17: 82,503,228-82,676,977 , GRCh37.p13 chr17: 80,461,104-80,634,853 RAB40B, MIR4525, 4 more genes
    nsv7063392inversion1nstd229human GRCh38 chr17: 82,609,707-82,780,313 , GRCh37.p13 chr17: 80,567,583-80,738,189 RAB40B, FN3KRP, 5 more genes
    nsv6997291copy number variation1nstd229human GRCh38 chr17: 82,591,776-82,674,032 , GRCh37.p13 chr17: 80,549,652-80,631,908 MIR4525, WDR45B, 2 more genes
    nsv6996190copy number variation1nstd229human GRCh38 chr17: 82,674,458-82,700,407 , GRCh37.p13 chr17: 80,632,334-80,658,283 RAB40B
    nsv6995894copy number variation1nstd229human GRCh38 chr17: 82,528,831-82,827,183 , GRCh37.p13 chr17: 80,486,707-80,785,059 LOC105371942, FN3KRP, 8 more genes
    nsv6995527copy number variation1nstd229human GRCh38 chr17: 82,681,594-82,916,948 , GRCh37.p13 chr17: 80,639,470-80,874,824 LOC101929552, TBCD, 4 more genes
    nsv6994562copy number variation1nstd229human GRCh38 chr17: 82,678,301-82,686,400 , GRCh37.p13 chr17: 80,636,177-80,644,276 RAB40B
    nsv6993283copy number variation1nstd229human GRCh38 chr17: 82,667,675-82,669,010 , GRCh37.p13 chr17: 80,625,551-80,626,886 MIR4525, RAB40B
    nsv6991740copy number variation1nstd229human GRCh38 chr17: 82,693,801-82,695,700 , GRCh37.p13 chr17: 80,651,677-80,653,576 RAB40B
    nsv6988391copy number variation1nstd229human GRCh38 chr17: 82,624,601-82,695,800 , GRCh37.p13 chr17: 80,582,477-80,653,676 MIR4525, RAB40B, 1 more genes
    nsv6985281copy number variation1nstd229human GRCh38 chr17: 82,654,201-82,957,097 , GRCh37.p13 chr17: 80,612,077-80,914,973 B3GNTL1, MIR4525, 6 more genes
    nsv6983693copy number variation1nstd229human GRCh38 chr17: 82,697,149-82,736,865 , GRCh37.p13 chr17: 80,655,025-80,694,741 RAB40B, FN3K, 2 more genes
    nsv6637647copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,585,033-81,041,938 , GRCh38.p12 chr17: 82,627,157-83,084,062 ZNF750, FN3KRP, 8 more genes
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