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Items: 1 to 20 of 364

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055423inversion1nstd229human GRCh38 chr4: 164,775,658-165,238,157 , GRCh37.p13 chr4: 165,696,810-166,159,309 TRIM61, SMIM31, 17 more genes
    nsv7052479inversion1nstd229human GRCh38 chr4: 164,757,556-164,759,128 , GRCh37.p13 chr4: 165,678,708-165,680,280 SMIM31
    nsv7051814inversion1nstd229human GRCh38 chr4: 164,790,724-164,790,754 , GRCh37.p13 chr4: 165,711,876-165,711,906 SMIM31
    nsv7043642inversion1nstd229human GRCh38 chr4: 164,754,516-164,759,324 , GRCh37.p13 chr4: 165,675,668-165,680,476 SMIM31
    nsv6758022copy number variation1nstd229human GRCh38 chr4: 164,793,778-164,800,274 , GRCh37.p13 chr4: 165,714,930-165,721,426 SMIM31
    nsv6754297copy number variation1nstd229human GRCh38 chr4: 164,584,468-164,988,469 , GRCh37.p13 chr4: 165,505,620-165,909,621 NACA3P, RNU6-284P, 11 more genes
    nsv6751864copy number variation1nstd229human GRCh38 chr4: 164,039,828-165,202,299 , GRCh37.p13 chr4: 164,960,980-166,123,451 LOC391711, TRIM75, 21 more genes
    nsv6751820copy number variation1nstd229human GRCh38 chr4: 164,784,634-165,203,278 , GRCh37.p13 chr4: 165,705,786-166,124,430 LOC100420385, TRIM60, 16 more genes
    nsv6750623copy number variation1nstd229human GRCh38 chr4: 164,776,894-165,258,284 , GRCh37.p13 chr4: 165,698,046-166,179,436 TMEM192, TRIM75, 18 more genes
    nsv6750028copy number variation1nstd229human GRCh38 chr4: 164,792,917-164,799,082 , GRCh37.p13 chr4: 165,714,069-165,720,234 SMIM31
    nsv6744904copy number variation1nstd229human GRCh38 chr4: 164,756,476-164,761,700 , GRCh37.p13 chr4: 165,677,628-165,682,852 SMIM31
    nsv6742919copy number variation1nstd229human GRCh38 chr4: 164,687,458-164,783,531 , GRCh37.p13 chr4: 165,608,610-165,704,683 SMIM31, CHORDC1P3
    nsv6740482copy number variation1nstd229human GRCh38 chr4: 164,057,383-165,303,005 , GRCh37.p13 chr4: 164,978,535-166,224,157 TRIM60P14, LOC391711, 24 more genes
    nsv6739948copy number variation1nstd229human GRCh38 chr4: 164,773,450-164,779,105 , GRCh37.p13 chr4: 165,694,602-165,700,257 SMIM31
    nsv6636318copy number variation1nstd102humanUncertain significance GRCh37 chr4: 161,461,677-166,911,259 , GRCh38.p12 chr4: 160,540,525-165,990,107 LOC107986325, NACA3P, 60 more genes
    nsv6636305copy number variation1nstd102humanUncertain significance GRCh37 chr4: 165,149,918-165,787,022 , GRCh38.p12 chr4: 164,228,766-164,865,870 MARCHF1, SMIM31, 3 more genes
    nsv6636254copy number variation1nstd102humanUncertain significance GRCh37 chr4: 164,980,534-166,223,066 , GRCh38.p12 chr4: 164,059,382-165,301,914 ANP32CP, GK3, 24 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6563016inversion1nstd223human GRCh38 chr4: 164,782,019-164,782,611 , GRCh37.p13 chr4: 165,703,171-165,703,763 SMIM31
    nsv6560559inversion1nstd223human GRCh38 chr4: 164,754,856-164,755,125 , GRCh37.p13 chr4: 165,676,008-165,676,277 SMIM31
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