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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4860026copy number variation1nstd200human GRCh37 chr18: 65,215,971-65,223,318 , GRCh38.p12 chr18: 67,548,734-67,556,081 , GRCh38.p12 chr18|NW_003315960.1: 194,461-198,278 DSEL-AS1
    nsv4860025copy number variation1nstd200human GRCh37 chr18: 65,186,955-65,191,259 , GRCh38.p12 chr18: 67,519,718-67,524,022 , GRCh38.p12 chr18|NW_003315960.1: 165,445-169,749 DSEL-AS1
    nsv4860024copy number variation1nstd200human GRCh37 chr18: 65,159,236-65,170,971 , GRCh38.p12 chr18: 67,491,999-67,503,734 , GRCh38.p12 chr18|NW_003315960.1: 137,726-149,461 0
    nsv4860023copy number variation1nstd200human GRCh37 chr18: 65,106,858-65,110,382 , GRCh38.p12 chr18: 67,439,621-67,443,145 , GRCh38.p12 chr18|NW_003315960.1: 15,887-19,411 0
    nsv4860022copy number variation1nstd200human GRCh37 chr18: 65,063,186-65,451,024 , GRCh38.p12 chr18: 67,395,949-67,783,787 , GRCh38.p12 chr18|NW_003315960.1: 1-198,278 DSEL, DSEL-AS1, 4 more genes
    nsv4768460insertion1nstd186human GRCh37 chr18: 65,121,218-65,121,218 , GRCh38.p12 chr18|NW_003315960.1: 30,247-30,247 , GRCh38.p12 chr18: 67,453,981-67,453,981 0
    nsv4754016insertion1nstd199human GRCh37 chr18: 65,121,222-65,121,222 , GRCh38.p12 chr18: 67,453,985-67,453,985 , GRCh38.p12 chr18|NW_003315960.1: 99,712-99,712 0
    nsv4717658mobile element insertion1nstd186human GRCh37 chr18: 65,138,854-65,138,854 , GRCh38.p12 chr18|NW_003315960.1: 117,345-117,345 , GRCh38.p12 chr18: 67,471,617-67,471,617 0
    nsv4689528mobile element insertion1nstd186human GRCh37 chr18: 65,138,862-65,138,862 , GRCh38.p12 chr18|NW_003315960.1: 117,353-117,353 , GRCh38.p12 chr18: 67,471,625-67,471,625 0
    nsv4685504insertion1nstd194human GRCh37 chr18: 65,121,218-65,121,218 , GRCh38.p12 chr18: 67,453,981-67,453,981 , GRCh38.p12 chr18|NW_003315960.1: 30,247-30,247 0
    nsv4627060copy number variation1nstd183human GRCh37 chr18: 65,162,560-65,168,109 , GRCh38.p12 chr18: 67,495,323-67,500,872 , GRCh38.p12 chr18|NW_003315960.1: 141,050-146,599 0
    nsv4619758copy number variation1nstd183human GRCh37 chr18: 65,063,229-65,446,018 , GRCh38.p12 chr18: 67,395,992-67,778,781 , GRCh38.p12 chr18|NW_003315960.1: 1-198,278 DSEL, DSEL-AS1, 4 more genes
    nsv4569308sequence alteration1nstd166human GRCh37.p13 chr18: 65,212,007-65,220,547 , GRCh38.p12 chr18: 67,544,770-67,553,310 , GRCh38.p12 chr18|NW_003315960.1: 190,497-198,278 DSEL-AS1
    nsv4567564mobile element insertion1nstd166human GRCh37.p13 chr18: 65,172,484-65,172,484 , GRCh38.p12 chr18|NW_003315960.1: 150,974-150,974 , GRCh38.p12 chr18: 67,505,247-67,505,247 DSEL
    nsv4560889mobile element insertion1nstd166human GRCh37.p13 chr18: 65,096,192-65,096,192 , GRCh38.p12 chr18: 67,428,955-67,428,955 , GRCh38.p12 chr18|NW_003315960.1: 5,233-5,233 0
    nsv4547186insertion1nstd166human GRCh37.p13 chr18: 65,093,424-65,093,424 , GRCh38.p12 chr18: 67,426,187-67,426,187 , GRCh38.p12 chr18|NW_003315960.1: 2,465-2,465 0
    nsv4513331mobile element insertion1nstd166human GRCh37.p13 chr18: 65,138,854-65,138,854 , GRCh38.p12 chr18|NW_003315960.1: 117,345-117,345 , GRCh38.p12 chr18: 67,471,617-67,471,617 0
    nsv4508016mobile element insertion1nstd166human GRCh37.p13 chr18: 65,158,889-65,158,889 , GRCh38.p12 chr18: 67,491,652-67,491,652 , GRCh38.p12 chr18|NW_003315960.1: 137,379-137,379 0
    nsv4505924mobile element insertion1nstd166human GRCh37.p13 chr18: 65,141,851-65,141,851 , GRCh38.p12 chr18|NW_003315960.1: 120,342-120,342 , GRCh38.p12 chr18: 67,474,614-67,474,614 0
    nsv4457527copy number variation1nstd102humanUncertain significance GRCh37 chr18: 65,063,532-65,453,697 , GRCh38.p12 chr18: 67,396,295-67,786,460 , GRCh38.p12 chr18|NW_003315960.1: 1-198,278 LOC105372173, LOC100129135, 5 more genes
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