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 120

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4684161copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881 TLR10, WDR1, 669 more genes
    nsv4674378copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859 USP17L30, LOC100422637, 394 more genes
    nsv4674196copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 5,914,109-17,264,668 , GRCh38.p12 chr4: 5,912,382-17,263,045 NKX3-2, BST1, 193 more genes
    nsv4673983copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-27,423,424 , GRCh38.p12 chr4: 68,453-27,421,802 LOC101928306, LINC02261, 439 more genes
    nsv4578568copy number variation1nstd102humanUncertain significance GRCh37 chr4: 13,529,798-22,750,583 , GRCh38.p12 chr4: 13,528,174-22,748,960 RPL21P46, LOC107986187, 88 more genes
    nsv4353435inversion1nstd102humanPathogenic GRCh38 chr4: 8,398,067-17,505,522 , GRCh37.p13 chr4: 8,399,794-17,507,145 NKX3-2, BST1, 152 more genes
    nsv4347528copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,778,849-27,760,141 , GRCh38.p12 chr4: 12,777,225-27,758,519 MTCO3P44, LINC01097, 148 more genes
    nsv4092550copy number variation1nstd166human GRCh37.p13 chr4: 16,304,488-16,383,919 , GRCh38.p12 chr4: 16,302,865-16,382,296 LOC100421364, ZEB2P1
    nsv3923296copy number variation1nstd102humanPathogenic GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931 OR7E99P, FBXL5, 446 more genes
    nsv3922899copy number variation1nstd102humanPathogenic NCBI36 chr4: 13,671,851-19,732,555 , GRCh37 chr4: 14,062,753-20,123,457 , GRCh38 chr4: 14,061,129-20,121,834 CD38, LOC105374513, 58 more genes
    nsv3917447copy number variation1nstd102humanPathogenic NCBI36 chr4: 4,479,031-17,071,270 , GRCh38 chr4: 4,426,403-17,460,549 , GRCh37 chr4: 4,428,130-17,462,172 SNORD162, MTND2P31, 218 more genes
    nsv3916848copy number variation1nstd102humanPathogenic GRCh37 chr4: 36,424-47,493,612 , GRCh38 chr4: 36,424-47,491,595 , NCBI36 chr4: 26,424-47,188,369 MIR943, LOC105374340, 634 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