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Items: 1 to 20 of 177

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    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
    nsv5615771insertion1nstd207human GRCh38 chr4: 6,638,383-6,638,383 , GRCh37.p13 chr4: 6,640,110-6,640,110 MRFAP1
    nsv5453796copy number variation1nstd206human GRCh38 chr4: 4,427,625-9,008,826 , GRCh37.p13 chr4: 4,429,352-9,010,552 , CPZ, 81 more genes
    nsv4925221copy number variation1nstd200human GRCh38 chr4: 6,643,161-6,645,271 , GRCh37.p13 chr4: 6,644,888-6,646,998 MRFAP1
    nsv4805225copy number variation1nstd200human GRCh37 chr4: 6,644,888-6,646,998 , GRCh38.p12 chr4: 6,643,161-6,645,271 MRFAP1
    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
    nsv4716435copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 2,909,440-6,871,516 , GRCh38.p12 chr4: 2,907,713-6,869,789 ADD1, ADRA2C, 83 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
    nsv4680715copy number variation1nstd189human GRCh37.p13 chr4: 6,446,590-6,810,920 , GRCh38.p12 chr4: 6,444,863-6,809,193 PPP2R2C, S100P, 11 more genes
    nsv4674429copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-6,984,507 , GRCh38.p12 chr4: 68,453-6,982,780 STX18-IT1, SLC26A1, 170 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
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