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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6727443copy number variation1nstd229human GRCh38 chr3: 148,836,793-148,844,091 , GRCh37.p13 chr3: 148,554,580-148,561,878 CPB1
    nsv6726790copy number variation1nstd229human GRCh38 chr3: 148,859,801-148,871,300 , GRCh37.p13 chr3: 148,577,588-148,589,087 CPB1, CPA3
    nsv6725058copy number variation1nstd229human GRCh38 chr3: 148,835,801-148,839,200 , GRCh37.p13 chr3: 148,553,588-148,556,987 CPB1
    nsv6721449copy number variation1nstd229human GRCh38 chr3: 148,857,567-148,857,635 , GRCh37.p13 chr3: 148,575,354-148,575,422 CPB1
    nsv6720890copy number variation1nstd229human GRCh38 chr3: 148,849,015-148,849,334 , GRCh37.p13 chr3: 148,566,802-148,567,121 CPB1
    nsv6718951copy number variation1nstd229human GRCh38 chr3: 148,846,647-148,849,690 , GRCh37.p13 chr3: 148,564,434-148,567,477 CPB1
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6636514copy number variation1nstd102humanUncertain significance GRCh37 chr3: 148,498,814-148,767,065 , GRCh38.p12 chr3: 148,781,027-149,049,278 CPA3, UBQLN4P1, 5 more genes
    nsv6560862inversion1nstd223human GRCh38 chr3: 148,850,328-148,851,062 , GRCh37.p13 chr3: 148,568,115-148,568,849 CPB1
    nsv6557916inversion1nstd223human GRCh38 chr3: 148,850,494-148,851,201 , GRCh37.p13 chr3: 148,568,281-148,568,988 CPB1
    nsv6365332copy number variation1nstd223human GRCh38 chr3: 148,849,015-148,849,323 , GRCh37.p13 chr3: 148,566,802-148,567,110 CPB1
    nsv6362681copy number variation1nstd223human GRCh38 chr3: 148,860,102-148,860,564 , GRCh37.p13 chr3: 148,577,889-148,578,351 CPB1
    nsv6362412copy number variation1nstd223human GRCh38 chr3: 148,845,245-148,846,156 , GRCh37.p13 chr3: 148,563,032-148,563,943 CPB1
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6311444copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709 TM4SF1, FKBP1AP4, 68 more genes
    nsv6294300mobile element insertion1nstd186human GRCh37 chr3: 148,544,002-148,544,053 , GRCh38.p12 chr3: 148,826,215-148,826,266 CPB1
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134997copy number variation1nstd213human GRCh37 chr3: 148,320,000-148,590,001 , GRCh38.p12 chr3: 148,602,213-148,872,214 AGTR1, CPA3, 3 more genes
    nsv6134994copy number variation1nstd213human GRCh37 chr3: 139,490,000-150,360,001 , GRCh38.p12 chr3: 139,771,158-150,642,214 , ATP1B3, 147 more genes
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