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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 PHF7, SEMA3G, 47 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv7055197inversion1nstd229human GRCh38 chr3: 52,426,847-52,608,000 , GRCh37.p13 chr3: 52,460,863-52,642,016 STAB1, PBRM1, 7 more genes
    nsv6716819copy number variation1nstd229human GRCh38 chr3: 52,514,797-52,536,674 , GRCh37.p13 chr3: 52,548,813-52,570,690 UQCC5, STAB1, 1 more genes
    nsv6369827copy number variation1nstd223human GRCh38 chr3: 52,164,358-54,467,618 , GRCh37.p13 chr3: 52,198,374-54,501,645 SEMA3G, STAB1, 61 more genes
    nsv6363355copy number variation1nstd223human GRCh38 chr3: 52,536,290-52,542,700 , GRCh37.p13 chr3: 52,570,306-52,576,716 UQCC5
    nsv6134815copy number variation1nstd213human GRCh37 chr3: 52,350,000-53,060,001 , GRCh38.p12 chr3: 52,315,984-53,025,985 ITIH1, ITIH3, 32 more genes
    nsv5902103copy number variation1nstd209human GRCh38 chr3: 52,538,348-52,538,407 , GRCh37.p13 chr3: 52,572,364-52,572,423 UQCC5
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5451666copy number variation1nstd206human GRCh38 chr3: 52,538,348-52,538,408 , GRCh37.p13 chr3: 52,572,364-52,572,424 UQCC5
    nsv5351766translocation1nstd200human GRCh38 chr3: 52,536,365-52,536,365 , GRCh38 chr3: 52,536,300-52,536,300 , GRCh37.p13 chr3: 52,570,316-52,570,316 , GRCh37.p13 chr3: 52,570,381-52,570,381 UQCC5
    nsv5343659translocation1nstd200human GRCh37 chr3: 52,572,364-52,572,364 , GRCh37 chr3: 52,572,424-52,572,424 , GRCh38.p12 chr3: 52,538,408-52,538,408 , GRCh38.p12 chr3: 52,538,348-52,538,348 UQCC5
    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
    nsv4911347copy number variation1nstd200human GRCh38 chr3: 51,769,352-52,724,007 , GRCh37.p13 chr3: 51,803,368-52,758,023 , ACY1, 55 more genes
    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
    nsv4790701copy number variation1nstd200human GRCh37 chr3: 51,803,368-52,758,023 , GRCh38.p12 chr3: 51,769,352-52,724,007 , SNORD19B, 55 more genes
    nsv4679783copy number variation1nstd189human GRCh37.p13 chr3: 52,082,781-53,128,685 , GRCh38.p12 chr3: 52,048,765-53,094,669 , ALAS1, 50 more genes
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 RRP9, LOC100301990, 76 more genes
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