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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7041592inversion1nstd229human GRCh38 chr3: 53,073,956-53,208,095 , GRCh37.p13 chr3: 53,107,972-53,185,061 PRKCD, RFT1
    nsv7041270inversion1nstd229human GRCh38 chr3: 52,619,221-53,173,329 , GRCh37.p13 chr3: 52,653,237-53,185,061 SNORD19, SNORD19C, 23 more genes
    nsv7040049inversion1nstd229human GRCh38 chr3: 52,838,316-53,173,499 , GRCh37.p13 chr3: 52,872,332-53,185,061 SFMBT1, SERBP1P3, 5 more genes
    nsv6717609copy number variation1nstd229human GRCh38 chr3: 53,113,856-53,320,010 , GRCh37.p13 chr3: 53,185,062-53,354,037 , GRCh37.p13 chr3|NW_004775426.1: 1-168,965 LOC107986087, RFT1, 3 more genes
    nsv6715311copy number variation1nstd229human GRCh38 chr3: 53,166,201-53,172,900 , GRCh37.p13 chr3|NW_004775426.1: 15,156-21,855 , GRCh37.p13 chr3: 53,200,217-53,206,916 PRKCD
    nsv6712502copy number variation1nstd229human GRCh38 chr3: 52,907,701-53,526,800 , GRCh37.p13 chr3: 52,941,717-53,560,827 SNORD38C, LOC107986087, 9 more genes
    nsv6711820copy number variation1nstd229human GRCh38 chr3: 53,045,076-53,183,112 , GRCh37.p13 chr3: 53,079,092-53,185,061 SERBP1P3, SFMBT1, 2 more genes
    nsv6699023copy number variation1nstd229human GRCh38 chr3: 52,811,798-54,282,378 , GRCh37.p13 chr3: 52,845,814-54,316,405 LOC105377095, SERBP1P3, 22 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
    nsv6367735copy number variation1nstd223human GRCh38 chr3: 52,941,201-53,367,100 , GRCh37.p13 chr3|NW_004775426.1: 1-216,055 , GRCh37.p13 chr3: 53,185,062-53,401,127 TKT, DCP1A, 7 more genes
    nsv6313569copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,968,525-53,450,333 , GRCh38.p12 chr3: 52,934,509-53,416,306 LOC105377094, SNORD38C, 7 more genes
    nsv5673485copy number variation1nstd102humanPathogenic GRCh37 chr3: 53,125,899-53,226,302 , GRCh38.p12 chr3: 53,091,883-53,192,286 PRKCD, RFT1
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5434110copy number variation1nstd206human GRCh38 chr3: 53,184,234-53,214,344 , GRCh37.p13 chr3|NW_004775426.1: 33,189-63,299 , GRCh37.p13 chr3: 53,218,250-53,248,360 PRKCD
    nsv5381422copy number variation1nstd102humanUncertain significance GRCh37 chr3: 53,125,899-53,215,768 , GRCh38.p12 chr3: 53,091,883-53,181,752 RFT1, PRKCD
    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
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