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Items: 1 to 20 of 134

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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
    nsv7041270inversion1nstd229human GRCh38 chr3: 52,619,221-53,173,329 , GRCh37.p13 chr3: 52,653,237-53,185,061 SNORD19, SNORD19C, 23 more genes
    nsv6716874copy number variation1nstd229human GRCh38 chr3: 52,619,220-52,838,314 , GRCh37.p13 chr3: 52,653,236-52,872,330 ITIH4-AS1, STIMATE, 18 more genes
    nsv6716471copy number variation1nstd229human GRCh38 chr3: 52,787,875-52,790,315 , GRCh37.p13 chr3: 52,821,891-52,824,331 ITIH1
    nsv6715302copy number variation1nstd229human GRCh38 chr3: 52,656,401-52,872,900 , GRCh37.p13 chr3: 52,690,417-52,906,916 SNORD136, GLT8D1, 19 more genes
    nsv6705478copy number variation1nstd229human GRCh38 chr3: 52,783,777-52,784,928 , GRCh37.p13 chr3: 52,817,793-52,818,944 ITIH1
    nsv6704476copy number variation1nstd229human GRCh38 chr3: 52,774,422-52,777,258 , GRCh37.p13 chr3: 52,808,438-52,811,274 ITIH1
    nsv6702214copy number variation1nstd229human GRCh38 chr3: 52,782,373-52,851,022 , GRCh37.p13 chr3: 52,816,389-52,885,038 ITIH3, MIR8064, 6 more genes
    nsv6636925copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,780,509-53,418,869 , GRCh38.p12 chr3: 52,746,493-53,384,842 LOC105377094, ITIH4-AS1, 17 more genes
    nsv6636758copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,783,975-53,418,893 , GRCh38.p12 chr3: 52,749,959-53,384,866 NEK4, MUSTN1, 17 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
    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
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    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
    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
    nsv4790730copy number variation1nstd200human GRCh37 chr3: 52,824,334-52,827,603 , GRCh38.p12 chr3: 52,790,318-52,793,587 ITIH3, ITIH1
    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
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