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Items: 1 to 20 of 239

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973691inversion1nstd209human GRCh38 chr6: 6,312,424-9,433,879 , GRCh37.p13 chr6: 6,312,657-9,434,112 , BMP6, 45 more genes
    nsv5896105copy number variation1nstd209human GRCh38 chr6: 7,548,083-10,446,730 , GRCh37.p13 chr6: 7,548,316-10,446,963 , TFAP2A-AS2, 37 more genes
    nsv5674021copy number variation1nstd102humanPathogenic GRCh37 chr6: 7,565,582-7,569,583 , GRCh38.p12 chr6: 7,565,349-7,569,350 DSP
    nsv5471779copy number variation1nstd206human GRCh38 chr6: 7,560,402-7,560,540 , GRCh37.p13 chr6: 7,560,635-7,560,773 DSP
    nsv5459084copy number variation1nstd206human GRCh38 chr6: 7,537,417-7,551,423 , GRCh37.p13 chr6: 7,537,650-7,551,656 DSP, DSP-AS1
    nsv5369210translocation1nstd200human GRCh38 chr8: 49,496,354-49,496,354 , GRCh38 chr6: 7,586,573-7,586,573 , GRCh37.p13 chr8: 50,408,913-50,408,913 , GRCh37.p13 chr6: 7,586,806-7,586,806 LOC100507464, DSP
    nsv5369209translocation1nstd200human GRCh38 chr8: 49,496,341-49,496,341 , GRCh38 chr6: 7,586,196-7,586,196 , GRCh37.p13 chr6: 7,586,429-7,586,429 , GRCh37.p13 chr8: 50,408,900-50,408,900 DSP, LOC100507464
    nsv5369208translocation1nstd200human GRCh38 chr6: 7,586,295-7,586,295 , GRCh38 chr6: 7,585,712-7,585,712 , GRCh37.p13 chr6: 7,586,528-7,586,528 , GRCh37.p13 chr6: 7,585,945-7,585,945 DSP
    nsv5306969copy number variation1nstd204human GRCh38.p13 chr6: 7,560,396-7,560,545 , GRCh37.p13 chr6: 7,560,629-7,560,778 DSP
    nsv5189573mobile element insertion1nstd203human GRCh38 chr6: 7,560,014-7,560,029 , GRCh37.p13 chr6: 7,560,247-7,560,262 DSP
    nsv4947611copy number variation1nstd200human GRCh38 chr6: 7,582,947-7,587,670 , GRCh37.p13 chr6: 7,583,180-7,587,903 DSP
    nsv4947610copy number variation1nstd200human GRCh38 chr6: 7,551,459-7,552,492 , GRCh37.p13 chr6: 7,551,692-7,552,725 DSP
    nsv4934392copy number variation1nstd200human GRCh38 chr6: 7,549,152-7,550,208 , GRCh37.p13 chr6: 7,549,385-7,550,441 DSP
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4809590copy number variation1nstd200human GRCh37 chr6: 7,583,180-7,587,903 , GRCh38.p12 chr6: 7,582,947-7,587,670 DSP
    nsv4809589copy number variation1nstd200human GRCh37 chr6: 7,551,689-7,552,727 , GRCh38.p12 chr6: 7,551,456-7,552,494 DSP
    nsv4729577copy number variation1nstd102humanUncertain significance GRCh37 chr6: 6,495,789-8,070,987 , GRCh38.p12 chr6: 6,495,556-8,070,754 LOC105374904, RPS26P29, 30 more genes
    nsv4706073copy number variation1nstd195human GRCh37 chr6: 7,554,362-7,554,363 , GRCh38.p12 chr6: 7,554,129-7,554,130 DSP
    nsv4682590copy number variation1nstd102humanPathogenic GRCh37 chr6: 7,570,660-7,586,121 , GRCh38.p12 chr6: 7,570,427-7,585,888 DSP
    nsv4679417copy number variation1nstd189human GRCh37.p13 chr6: 7,551,462-7,883,473 , GRCh38.p12 chr6: 7,551,229-7,883,240 , BMP6, 6 more genes
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