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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974999inversion1nstd209human GRCh38 chr6: 8,309,480-8,919,987 , GRCh37.p13 chr6: 8,309,713-8,920,220 , SLC35B3, 3 more genes
    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
    nsv5845742copy number variation1nstd209human GRCh38 chr6: 8,653,701-8,654,792 , GRCh37.p13 chr6: 8,653,934-8,655,025 LOC100506207, HULC
    nsv5718327mobile element insertion2nstd211human GRCh38 chr6: 8,654,075-8,654,075 , GRCh37.p13 chr6: 8,654,308-8,654,308 LOC100506207, HULC
    nsv5464463copy number variation1nstd206human GRCh38 chr6: 8,592,371-8,718,959 , GRCh37.p13 chr6: 8,592,604-8,719,192 HULC, LOC100506207
    nsv5458315copy number variation1nstd206human GRCh38 chr6: 8,650,691-8,654,018 , GRCh37.p13 chr6: 8,650,924-8,654,251 LOC100506207, HULC
    nsv4947667copy number variation1nstd200human GRCh38 chr6: 8,647,310-8,666,038 , GRCh37.p13 chr6: 8,647,543-8,666,271 LOC100506207, HULC
    nsv4947662copy number variation1nstd200human GRCh38 chr6: 8,592,371-8,718,959 , GRCh37.p13 chr6: 8,592,604-8,719,192 HULC, LOC100506207
    nsv4934398copy number variation1nstd200human GRCh38 chr6: 8,579,603-9,945,262 , GRCh37.p13 chr6: 8,579,836-9,945,495 , OFCC1, 5 more genes
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4828483copy number variation1nstd200human GRCh37 chr6: 8,579,836-9,945,495 , GRCh38.p12 chr6: 8,579,603-9,945,262 , OFCC1, 5 more genes
    nsv4674883copy number variation1nstd102humanUncertain significance GRCh37 chr6: 8,286,885-10,039,004 , GRCh38.p12 chr6: 8,286,652-10,038,771 LOC105374911, LOC105374914, 6 more genes
    nsv4598694copy number variation1nstd183human GRCh37 chr6: 8,592,499-8,719,124 , GRCh38.p12 chr6: 8,592,266-8,718,891 LOC100506207, HULC
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4402710copy number variation1nstd174human GRCh37 chr6: 8,654,394-8,724,508 , GRCh38.p12 chr6: 8,654,161-8,724,275 HULC, LOC100506207
    nsv4398976copy number variation1nstd174human GRCh37 chr6: 8,589,525-8,722,717 , GRCh38.p12 chr6: 8,589,292-8,722,484 LOC100506207, HULC
    nsv4380237copy number variation2nstd173human GRCh37 chr6: 8,594,605-8,718,988 , GRCh38.p12 chr6: 8,594,372-8,718,755 HULC, LOC100506207
    nsv4130954copy number variation1nstd166human GRCh37.p13 chr6: 8,648,909-8,657,920 , GRCh38.p12 chr6: 8,648,676-8,657,687 LOC100506207, HULC
    nsv4121143copy number variation1nstd166human GRCh37.p13 chr6: 8,592,604-8,719,192 , GRCh38.p12 chr6: 8,592,371-8,718,959 HULC, LOC100506207
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