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Items: 1 to 20 of 92

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057899inversion1nstd229human GRCh38 chr3: 32,727,416-33,178,209 , GRCh37.p13 chr3: 32,768,908-33,219,701 TRIM71, TMPPE, 11 more genes
    nsv7046617inversion1nstd229human GRCh38 chr3: 32,574,554-33,118,910 , GRCh37.p13 chr3: 32,616,046-33,160,402 GLB1, LOC107986072, 12 more genes
    nsv6711948copy number variation1nstd229human GRCh38 chr3: 32,782,346-32,811,493 , GRCh37.p13 chr3: 32,823,838-32,852,985 RPL23AP43
    nsv6709849copy number variation1nstd229human GRCh38 chr3: 32,786,193-32,793,203 , GRCh37.p13 chr3: 32,827,685-32,834,695 RPL23AP43
    nsv6700642copy number variation1nstd229human GRCh38 chr3: 32,689,055-32,896,442 , GRCh37.p13 chr3: 32,730,547-32,937,934 CNOT10, RPL23AP43, 2 more genes
    nsv6538216inversion1nstd223human GRCh38 chr3: 32,784,440-32,785,300 , GRCh37.p13 chr3: 32,825,932-32,826,792 RPL23AP43
    nsv6366741copy number variation1nstd223human GRCh38 chr3: 32,766,601-32,847,400 , GRCh37.p13 chr3: 32,808,093-32,888,892 CNOT10, RPL23AP43, 1 more genes
    nsv6313891copy number variation1nstd102humanUncertain significance GRCh37 chr3: 31,859,973-33,127,072 , GRCh38.p12 chr3: 31,818,481-33,085,580 RPL30P4, RPL21P40, 22 more genes
    nsv6313757copy number variation1nstd102humanUncertain significance GRCh37 chr3: 32,699,328-35,286,114 , GRCh38.p12 chr3: 32,657,836-35,244,622 CRTAP, FECHP1, 26 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6134843copy number variation1nstd213human GRCh37 chr3: 31,580,000-32,830,001 , GRCh38.p12 chr3: 31,538,508-32,788,509 GPD1L, CNOT10, 19 more genes
    nsv5993324copy number variation1nstd212human GRCh38 chr3: 32,783,818-32,783,931 , GRCh37.p13 chr3: 32,825,310-32,825,423 RPL23AP43
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4927160copy number variation1nstd200human GRCh38 chr3: 32,784,159-32,791,274 , GRCh37.p13 chr3: 32,825,651-32,832,766 RPL23AP43
    nsv4924313copy number variation1nstd200human GRCh38 chr3: 32,786,193-32,793,203 , GRCh37.p13 chr3: 32,827,685-32,834,695 RPL23AP43
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4793924copy number variation1nstd200human GRCh37 chr3: 32,827,684-32,834,696 , GRCh38.p12 chr3: 32,786,192-32,793,204 RPL23AP43
    nsv4793920copy number variation1nstd200human GRCh37 chr3: 32,391,980-33,567,070 , GRCh38.p12 chr3: 32,350,488-33,525,578 , RPL30P4, 25 more genes
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