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Items: 1 to 20 of 389

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140569insertion1nstd232human GRCh37.p13 chr6: 71,442,214-71,442,214 , GRCh38.p12 chr6: 70,732,511-70,732,511 SMAP1
    nsv7044663inversion1nstd229human GRCh38 chr6: 70,000,614-70,911,384 , GRCh37.p13 chr6: 70,710,506-71,621,087 COL9A1, SDHAF4, 14 more genes
    nsv7044140inversion1nstd229human GRCh38 chr6: 70,804,381-70,927,502 , GRCh37.p13 chr6: 71,514,084-71,637,205 LOC105377850, B3GAT2, 1 more genes
    nsv6797628copy number variation1nstd229human GRCh38 chr6: 70,780,101-70,812,800 , GRCh37.p13 chr6: 71,489,804-71,522,503 SMAP1
    nsv6795386copy number variation1nstd229human GRCh38 chr6: 70,690,601-70,732,400 , GRCh37.p13 chr6: 71,400,304-71,442,103 LOC100419975, SMAP1
    nsv6794957copy number variation1nstd229human GRCh38 chr6: 70,737,757-70,750,125 , GRCh37.p13 chr6: 71,447,460-71,459,828 SMAP1
    nsv6794861copy number variation1nstd229human GRCh38 chr6: 70,775,901-70,918,200 , GRCh37.p13 chr6: 71,485,604-71,627,903 SMAP1, B3GAT2, 1 more genes
    nsv6793012copy number variation1nstd229human GRCh38 chr6: 70,766,301-70,767,300 , GRCh37.p13 chr6: 71,476,004-71,477,003 SMAP1
    nsv6790912copy number variation1nstd229human GRCh38 chr6: 70,723,275-70,724,248 , GRCh37.p13 chr6: 71,432,978-71,433,951 SMAP1
    nsv6789208copy number variation1nstd229human GRCh38 chr6: 70,714,587-70,804,047 , GRCh37.p13 chr6: 71,424,290-71,513,750 SMAP1
    nsv6789159copy number variation1nstd229human GRCh38 chr6: 70,770,672-70,770,710 , GRCh37.p13 chr6: 71,480,375-71,480,413 SMAP1
    nsv6786111copy number variation1nstd229human GRCh38 chr6: 70,723,301-70,737,900 , GRCh37.p13 chr6: 71,433,004-71,447,603 SMAP1
    nsv6785408copy number variation1nstd229human GRCh38 chr6: 70,847,858-70,850,359 , GRCh37.p13 chr6: 71,557,561-71,560,062 SMAP1
    nsv6782680copy number variation1nstd229human GRCh38 chr6: 70,818,924-70,819,904 , GRCh37.p13 chr6: 71,528,627-71,529,607 SMAP1
    nsv6780113copy number variation1nstd229human GRCh38 chr6: 70,800,891-70,800,947 , GRCh37.p13 chr6: 71,510,594-71,510,650 SMAP1
    nsv6779941copy number variation1nstd229human GRCh38 chr6: 70,823,791-70,826,152 , GRCh37.p13 chr6: 71,533,494-71,535,855 SMAP1
    nsv6779329copy number variation1nstd229human GRCh38 chr6: 70,810,802-70,929,840 , GRCh37.p13 chr6: 71,520,505-71,639,543 SMAP1, LOC105377850, 1 more genes
    nsv6778512copy number variation1nstd229human GRCh38 chr6: 70,658,797-70,667,534 , GRCh37.p13 chr6: 71,368,500-71,377,237 SLC25A6P6, SMAP1
    nsv6636629copy number variation1nstd102humanUncertain significance GRCh37 chr6: 70,320,224-71,568,417 , GRCh38.p12 chr6: 69,610,332-70,858,714 COL19A1, LOC105377848, 16 more genes
    nsv6634377copy number variation1nstd102humanPathogenic GRCh37 chr6: 71,105,038-75,200,617 , GRCh38.p12 chr6: 70,395,335-74,490,901 TXNP7, MTO1, 63 more genes
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