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Items: 1 to 20 of 78

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7060956inversion1nstd229human GRCh38 chr10: 17,641,498-17,641,544 , GRCh37.p13 chr10|NW_003315932.1: 70,289-70,335 , GRCh37.p13 chr10: 17,683,497-17,683,543 STAM-DT
    nsv6887313copy number variation1nstd229human GRCh38 chr10: 17,600,001-17,646,900 , GRCh37.p13 chr10|NW_003315932.1: 28,792-75,691 , GRCh37.p13 chr10: 17,642,000-17,688,899 STAM-DT, HACD1, 1 more genes
    nsv6887279copy number variation1nstd229human GRCh38 chr10: 17,640,871-17,775,138 , GRCh37.p13 chr10: 17,682,870-18,064,127 , GRCh37.p13 chr10|NW_003315932.1: 69,662-203,929 STAM-DT, STAM, 1 more genes
    nsv6886668copy number variation1nstd229human GRCh38 chr10: 17,607,297-18,187,851 , GRCh37.p13 chr10|NW_003315932.1: 36,088-392,792 , GRCh37.p13 chr10: 17,649,296-18,252,930 STAM, TMEM236, 7 more genes
    nsv6885205copy number variation1nstd229human GRCh38 chr10: 17,633,912-17,700,830 , GRCh37.p13 chr10: 17,675,911-17,742,829 , GRCh37.p13 chr10|NW_003315932.1: 62,703-129,621 STAM-DT, STAM
    nsv6881697copy number variation1nstd229human GRCh38 chr10: 17,602,801-17,639,600 , GRCh37.p13 chr10|NW_003315932.1: 31,592-68,391 , GRCh37.p13 chr10: 17,644,800-17,681,599 STAM-DT, HACD1
    nsv6637955copy number variation1nstd102humanUncertain significance GRCh37 chr10: 17,376,968-18,486,923 , GRCh38.p12 chr10: 17,334,969-18,197,994 TMEM236, MRC1, 12 more genes
    nsv6620107copy number variation1nstd224human GRCh37 chr10: 17,670,032-17,737,047 , GRCh38.p12 chr10: 17,628,033-17,695,048 STAM, STAM-DT
    nsv6443661copy number variation1nstd223human GRCh38 chr10: 17,639,548-17,641,050 , GRCh37.p13 chr10: 17,681,547-17,683,049 , GRCh37.p13 chr10|NW_003315932.1: 68,339-69,841 STAM-DT
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6308906copy number variation2nstd102humanUncertain significance GRCh37 chr10: 16,866,974-18,828,653 , GRCh38.p12 chr10: 16,824,975-18,539,724 TMEM236, SLC39A12-AS1, 18 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6131971copy number variation1nstd213human GRCh37 chr10: 7,450,000-17,830,001 , GRCh38.p12 chr10: 7,408,038-17,788,002 ATP5F1C, TRDMT1, 150 more genes
    nsv5960895insertion1nstd209human GRCh38 chr10: 17,639,402-17,639,402 , GRCh37.p13 chr10|NW_003315932.1: 68,193-68,193 , GRCh37.p13 chr10: 17,681,401-17,681,401 STAM-DT
    nsv5478932copy number variation1nstd206human GRCh38 chr10: 17,638,259-17,642,850 , GRCh37.p13 chr10|NW_003315932.1: 67,050-71,641 , GRCh37.p13 chr10: 17,680,258-17,684,849 STAM, STAM-DT
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4182809copy number variation1nstd166human GRCh37.p13 chr10: 17,680,258-17,684,849 , GRCh38.p12 chr10: 17,638,259-17,642,850 STAM, STAM-DT
    nsv3961226insertion1nstd168human GRCh38 chr10: 17,638,647-17,651,244 , GRCh37.p13 chr10|NW_003315932.1: 67,438-80,035 , GRCh37.p13 chr10: 17,680,646-17,693,243 STAM, STAM-DT
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