U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 217

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7061615inversion1nstd229human GRCh38 chr8: 139,238,401-143,070,465 , GRCh37.p13 chr8: 140,250,644-144,151,882 PEG13, LINC01300, 63 more genes
    nsv6876465copy number variation1nstd229human GRCh38 chr8: 142,576,274-142,610,957 , GRCh37.p13 chr8: 143,657,635-143,692,318 ARC
    nsv6871400copy number variation1nstd229human GRCh38 chr8: 142,558,701-142,684,700 , GRCh37.p13 chr8: 143,640,062-143,711,228 JRK, ARC, 3 more genes
    nsv6861295copy number variation1nstd229human GRCh38 chr8: 142,449,701-142,617,700 , GRCh37.p13 chr8: 143,531,062-143,699,061 MROH4P, ARC, 1 more genes
    nsv6858265copy number variation1nstd229human GRCh38 chr8: 142,571,201-142,615,200 , GRCh37.p13 chr8: 143,652,562-143,696,561 MROH4P, ARC
    nsv6637631copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,836,592-144,175,046 , GRCh38.p12 chr8: 141,755,231-143,093,629 CYP11B1, LOC105375792, 33 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632568copy number variation1nstd224human GRCh37 chr8: 143,639,470-144,398,219 , GRCh38.p12 chr8: 142,558,109-143,316,049 CYP11B2, GLI4, 33 more genes
    nsv6417526copy number variation1nstd223human GRCh38 chr8: 142,256,520-142,935,362 , GRCh37.p13 chr8: 143,337,881-144,016,778 ZNHIT1P1, MROH4P, 19 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313487copy number variation1nstd102humanPathogenic GRCh37 chr8: 130,863,093-146,295,771 , GRCh38.p12 chr8: 129,850,847-145,070,385 LOC105375784, CYP11B2, 253 more genes
    nsv6269188copy number variation1nstd214human GRCh38 chr8: 142,610,132-142,610,183 , GRCh37.p13 chr8: 143,691,493-143,691,544 ARC
    nsv6267746copy number variation1nstd214human GRCh38 chr8: 142,609,955-142,610,006 , GRCh37.p13 chr8: 143,691,316-143,691,367 ARC
    nsv6174895copy number variation1nstd214human GRCh38 chr8: 142,610,173-142,610,378 , GRCh37.p13 chr8: 143,691,534-143,691,739 ARC
    nsv6169195copy number variation1nstd214human GRCh38 chr8: 142,610,080-142,610,183 , GRCh37.p13 chr8: 143,691,441-143,691,544 ARC
    nsv6136341copy number variation1nstd213human GRCh37 chr8: 142,830,000-144,520,001 , GRCh38.p12 chr8: 141,748,639-143,437,831 PSCA, ZC3H3, 48 more genes
    nsv6071417insertion1nstd212human GRCh38 chr8: 142,610,019-142,610,019 , GRCh37.p13 chr8: 143,691,380-143,691,380 ARC
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center