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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7144582copy number variation1nstd232human GRCh37.p13 chr4: 41,263,815-41,263,889 , GRCh38.p12 chr4: 41,261,798-41,261,872 UCHL1
    nsv7137048copy number variation1nstd102humanPathogenic GRCh37 chr4: 40,337,485-41,941,400 , GRCh38.p12 chr4: 40,335,468-41,939,383 RNU6-1195P, RNU6-836P, 23 more genes
    nsv7057597inversion1nstd229human GRCh38 chr4: 40,706,162-41,294,144 , GRCh37.p13 chr4: 40,708,179-41,296,161 UCHL1-DT, UCHL1, 6 more genes
    nsv7054319inversion1nstd229human GRCh38 chr4: 40,437,339-43,087,585 , GRCh37.p13 chr4: 40,439,356-43,089,602 RN7SKP82, RPS7P7, 33 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6312251copy number variation1nstd102humanUncertain significance GRCh37 chr4: 38,765,721-41,750,627 , GRCh38.p12 chr4: 38,764,100-41,748,610 RNU6-32P, SMIM14-DT, 52 more genes
    nsv6135081copy number variation1nstd213human GRCh37 chr4: 39,770,000-41,280,001 , GRCh38.p12 chr4: 39,768,380-41,277,984 APBB2, RHOH, 22 more genes
    nsv5093588mobile element insertion1nstd203human GRCh38 chr4: 41,262,444-41,262,458 , GRCh37.p13 chr4: 41,264,461-41,264,475 UCHL1
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5037641inversion1nstd200human GRCh38 chr4: 40,706,162-41,294,144 , GRCh37.p13 chr4: 40,708,179-41,296,161 , APBB2, 7 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
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