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 98

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5377274translocation1nstd200human GRCh38 chr2: 78,879,140-78,879,140 , GRCh38 chr3: 102,755,272-102,755,272 , GRCh37.p13 chr2: 79,106,266-79,106,266 , GRCh37.p13 chr3: 102,474,116-102,474,116 RNU6-461P
    nsv5343149translocation1nstd200human GRCh37 chr3: 102,474,118-102,474,118 , GRCh37 chr2: 79,117,786-79,117,786 , GRCh38.p12 chr2: 78,890,660-78,890,660 , GRCh38.p12 chr3: 102,755,274-102,755,274 RNU6-461P
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4794247copy number variation1nstd200human GRCh37 chr3: 102,444,960-103,088,217 , GRCh38.p12 chr3: 102,726,116-103,369,373 NDUFA4P2, LOC105374017, 3 more genes
    nsv4674254copy number variation1nstd102humanPathogenic GRCh37 chr3: 101,812,245-112,174,485 , GRCh38.p12 chr3: 102,093,401-112,455,638 IFT57, LINC00636, 111 more genes
    nsv4079745copy number variation1nstd166human GRCh37.p13 chr3: 102,196,611-102,652,376 , GRCh38.p12 chr3: 102,477,767-102,933,532 ZPLD1, LOC105374016, 4 more genes
    nsv3924226copy number variation1nstd102humanLikely benign NCBI36 chr3: 103,869,485-104,432,220 , GRCh37 chr3: 102,386,795-102,949,530 , GRCh38 chr3: 102,667,951-103,230,686 LOC105374018, RNU1-43P, 3 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3917160copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903 ATP6V1A, RPS10P4, 297 more genes
    nsv3911724copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 95,021,157-105,090,283 , GRCh37 chr3: 93,538,467-103,607,593 , GRCh38 chr3: 93,819,623-103,888,749 COL8A1, CPOX, 132 more genes
    nsv3911662copy number variation1nstd102humanPathogenic NCBI36 chr3: 102,633,427-117,731,277 , GRCh37.p13 chr3: 101,150,737-116,248,587 , GRCh38.p12 chr3: 101,431,893-116,529,740 SIDT1, PPIAP15, 188 more genes
    nsv3910775copy number variation1nstd102humanPathogenic GRCh37 chr3: 97,514,213-115,382,196 , GRCh38 chr3: 97,795,369-115,663,349 , NCBI36 chr3: 98,996,903-116,864,886 ZBTB11-AS1, RABGGTBP1, 258 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3884686copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 100,613,996-108,976,446 , GRCh38.p12 chr3: 100,895,152-109,257,599 ALCAM, CBLB, 94 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3168801copy number variation1nstd158human GRCh37 chr3: 101,877,605-123,773,473 , GRCh38.p12 chr3: 102,158,761-124,054,626 , ADCY5, 303 more genes
    nsv2740810copy number variation1nstd130human NCBI36 chr3: 103,580,018-104,374,828 , GRCh37.p13 chr3: 102,097,328-102,892,138 , GRCh38.p12 chr3: 102,378,484-103,173,294 ZPLD1, LOC105374018, 5 more genes
    nsv2736104copy number variation1nstd130human NCBI36 chr3: 103,549,944-104,347,366 , GRCh37.p13 chr3: 102,067,254-102,864,676 , GRCh38.p12 chr3: 102,348,410-103,145,832 LOC105374017, LOC107986106, 4 more genes
    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