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Items: 1 to 20 of 187

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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
    nsv6755114copy number variation1nstd229human GRCh38 chr4: 164,917,438-164,917,638 , GRCh37.p13 chr4: 165,838,590-165,838,790 TRIM60P14
    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
    nsv6754113copy number variation1nstd229human GRCh38 chr4: 164,895,701-165,053,600 , GRCh37.p13 chr4: 165,816,853-165,974,752 TRIM61, LOC391711, 12 more genes
    nsv6752137copy number variation1nstd229human GRCh38 chr4: 164,870,625-164,948,338 , GRCh37.p13 chr4: 165,791,777-165,869,490 LOC391711, NACA3P, 5 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
    nsv6750700copy number variation1nstd229human GRCh38 chr4: 164,900,428-164,973,022 , GRCh37.p13 chr4: 165,821,580-165,894,174 NACA3P, LOC391711, 6 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
    nsv6742754copy number variation1nstd229human GRCh38 chr4: 164,895,154-164,918,604 , GRCh37.p13 chr4: 165,816,306-165,839,756 TRIM60P14, APELA, 1 more genes
    nsv6741245copy number variation1nstd229human GRCh38 chr4: 164,903,266-164,964,316 , GRCh37.p13 chr4: 165,824,418-165,885,468 TRIM61, RPL26P16, 6 more genes
    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
    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
    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
    nsv6629627copy number variation1nstd224human GRCh37 chr4: 165,836,060-166,110,819 , GRCh38.p12 chr4: 164,914,908-165,189,667 NACA3P, LOC391711, 13 more genes
    nsv6629575copy number variation1nstd224human GRCh37 chr4: 165,814,775-165,879,007 , GRCh38.p12 chr4: 164,893,623-164,957,855 FAM218A, NACA3P, 7 more genes
    nsv6629203copy number variation1nstd224human GRCh37 chr4: 165,827,749-165,879,007 , GRCh38.p12 chr4: 164,906,597-164,957,855 FAM218A, NACA3P, 6 more genes
    nsv6571433inversion1nstd223human GRCh38 chr4: 164,917,316-164,917,797 , GRCh37.p13 chr4: 165,838,468-165,838,949 TRIM60P14
    nsv6393456copy number variation1nstd223human GRCh38 chr4: 164,584,468-164,988,469 , GRCh37.p13 chr4: 165,505,620-165,909,621 LOC391710, APELA, 11 more genes
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