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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053413inversion1nstd229human GRCh38 chr4: 65,681,060-65,681,128 , GRCh37.p13 chr4: 66,546,778-66,546,846 EPHA5-AS1
    nsv6757735copy number variation1nstd229human GRCh38 chr4: 62,015,862-66,463,521 , GRCh37.p13 chr4: 62,881,580-67,329,239 EXOC5P1, MTCO3P28, 37 more genes
    nsv6756221copy number variation1nstd229human GRCh38 chr4: 65,582,672-65,677,910 , GRCh37.p13 chr4: 66,448,390-66,543,628 EPHA5-AS1, EPHA5
    nsv6755787copy number variation1nstd229human GRCh38 chr4: 65,675,525-65,696,602 , GRCh37.p13 chr4: 66,541,243-66,562,320 EPHA5-AS1
    nsv6755602copy number variation1nstd229human GRCh38 chr4: 65,689,231-65,690,475 , GRCh37.p13 chr4: 66,554,949-66,556,193 EPHA5-AS1
    nsv6754236copy number variation1nstd229human GRCh38 chr4: 65,676,207-65,685,805 , GRCh37.p13 chr4: 66,541,925-66,551,523 EPHA5-AS1
    nsv6746063copy number variation1nstd229human GRCh38 chr4: 65,688,993-65,691,853 , GRCh37.p13 chr4: 66,554,711-66,557,571 EPHA5-AS1
    nsv6736234copy number variation1nstd229human GRCh38 chr4: 57,957,083-67,107,892 , GRCh37.p13 chr4: 58,823,249-67,973,610 MTCYBP16, ADGRL3-AS1, 53 more genes
    nsv6636883copy number variation1nstd102humanUncertain significance GRCh37 chr4: 66,215,872-68,647,080 , GRCh38.p12 chr4: 65,350,154-67,781,362 LOC100419046, LOC105377260, 24 more genes
    nsv6629887copy number variation1nstd224human GRCh37 chr4: 66,511,949-66,797,440 , GRCh38.p12 chr4: 65,646,231-65,931,722 LOC105377259, EPHA5, 3 more genes
    nsv6560548inversion1nstd223human GRCh38 chr4: 65,676,248-65,676,338 , GRCh37.p13 chr4: 66,541,966-66,542,056 EPHA5-AS1
    nsv6395414copy number variation1nstd223human GRCh38 chr4: 65,506,303-67,062,808 , GRCh37.p13 chr4: 66,372,021-67,928,526 RNU2-40P, MIR1269A, 11 more genes
    nsv6393875copy number variation1nstd223human GRCh38 chr4: 65,684,701-65,686,100 , GRCh37.p13 chr4: 66,550,419-66,551,818 EPHA5-AS1
    nsv6389995copy number variation1nstd223human GRCh38 chr4: 65,689,870-65,690,547 , GRCh37.p13 chr4: 66,555,588-66,556,265 EPHA5-AS1
    nsv6387040copy number variation1nstd223human GRCh38 chr4: 65,688,087-65,688,552 , GRCh37.p13 chr4: 66,553,805-66,554,270 EPHA5-AS1
    nsv6382010copy number variation1nstd223human GRCh38 chr4: 65,687,501-65,688,500 , GRCh37.p13 chr4: 66,553,219-66,554,218 EPHA5-AS1
    nsv6376768copy number variation1nstd223human GRCh38 chr4: 65,684,396-65,684,942 , GRCh37.p13 chr4: 66,550,114-66,550,660 EPHA5-AS1
    nsv6375694copy number variation1nstd223human GRCh38 chr4: 65,680,401-65,691,500 , GRCh37.p13 chr4: 66,546,119-66,557,218 EPHA5-AS1
    nsv6313740copy number variation1nstd102humanPathogenic GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800 CXCL8, UGT2A1, 175 more genes
    nsv6307930mobile element insertion1nstd186human GRCh37 chr4: 66,556,238-66,556,240 , GRCh38.p12 chr4: 65,690,520-65,690,522 EPHA5-AS1
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