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 189

    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
    nsv5979532inversion1nstd209human GRCh38 chr4: 4,147,913-9,493,295 , GRCh37.p13 chr4: 4,149,640-9,494,939 , CRMP1, 130 more genes
    nsv5974394inversion1nstd209human GRCh38 chr4: 4,005,086-9,639,734 , GRCh37.p13 chr4: 4,006,813-9,641,358 , CRMP1, 142 more genes
    nsv5973087inversion1nstd209human GRCh38 chr4: 3,883,398-8,956,544 , GRCh37.p13 chr4: 3,885,125-8,958,270 , CRMP1, 102 more genes
    nsv5453796copy number variation1nstd206human GRCh38 chr4: 4,427,625-9,008,826 , GRCh37.p13 chr4: 4,429,352-9,010,552 , CPZ, 81 more genes
    nsv5434093copy number variation1nstd206human GRCh38 chr4: 7,434,883-7,434,993 , GRCh37.p13 chr4: 7,436,610-7,436,720 SORCS2, PSAPL1
    nsv4925236copy number variation1nstd200human GRCh38 chr4: 7,410,794-7,472,004 , GRCh37.p13 chr4: 7,412,521-7,473,731 PSAPL1, SORCS2, 1 more genes
    nsv4913117copy number variation1nstd200human GRCh38 chr4: 7,434,883-7,434,993 , GRCh37.p13 chr4: 7,436,610-7,436,720 PSAPL1, SORCS2
    nsv4799328copy number variation1nstd200human GRCh37 chr4: 7,436,610-7,436,720 , GRCh38.p12 chr4: 7,434,883-7,434,993 PSAPL1, SORCS2
    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
    nsv4674283copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-9,768,141 , GRCh38.p12 chr4: 68,453-9,766,517 MFSD10, PCGF3-AS1, 255 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
    nsv4674174copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-10,312,798 , GRCh38.p12 chr4: 68,453-10,311,174 RNA5SP153, NICOL1, 267 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