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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3876047copy number variation1nstd102humanLikely benign GRCh37 chr4: 81,506,519-81,686,491 , GRCh38.p12 chr4: 80,585,365-80,765,337 CFAP299
    nsv3924876copy number variation1nstd102humanBenign GRCh38 chr4: 80,772,092-80,879,777 , GRCh37 chr4: 81,693,246-81,800,931 , NCBI36 chr4: 81,912,270-82,019,955 CFAP299
    nsv3887873copy number variation1nstd102humanBenign GRCh37 chr4: 81,508,970-81,529,088 , GRCh38.p12 chr4: 80,587,816-80,607,934 CFAP299
    nsv3887182copy number variation1nstd102humanBenign GRCh37 chr4: 81,531,478-81,535,393 , GRCh38.p12 chr4: 80,610,324-80,614,239 CFAP299
    nsv6636641copy number variation1nstd102humanUncertain significance GRCh37 chr4: 81,444,078-81,918,621 , GRCh38.p12 chr4: 80,522,924-80,997,467 CFAP299
    nsv4729054copy number variation1nstd102humanUncertain significance GRCh37 chr4: 81,490,292-81,957,186 , GRCh38.p12 chr4: 80,569,138-81,036,032 CFAP299, BMP3
    nsv3876391copy number variation1nstd102humanLikely benign GRCh37 chr4: 81,186,787-81,563,339 , GRCh38.p12 chr4: 80,265,633-80,642,185 CFAP299, FGF5, 3 more genes
    nsv3879617copy number variation1nstd102humanUncertain significance GRCh37 chr4: 81,180,091-81,686,491 , GRCh38.p12 chr4: 80,258,937-80,765,337 CFAP299, FGF5, 3 more genes
    nsv4674704copy number variation1nstd102humanUncertain significance GRCh37 chr4: 81,191,045-81,563,339 , GRCh38.p12 chr4: 80,269,891-80,642,185 CFAP299, LOC100419739, 3 more genes
    nsv3923759copy number variation1nstd102humanPathogenic NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502 CFAP299, EREG, 530 more genes
    nsv3923733copy number variation1nstd102humanPathogenic GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621 CFAP299, PDLIM5, 215 more genes
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 CFAP299, LOC105377327, 214 more genes
    nsv4729598copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632 CFAP299, PTPN11P5, 244 more genes
    nsv3888958copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,314,915-96,636,651 , GRCh38.p12 chr4: 80,393,761-95,715,500 CFAP299, LOC391674, 156 more genes
    nsv6313484copy number variation1nstd102humanPathogenic GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074 CFAP299, LOC105377329, 166 more genes
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 CFAP299, MICOS10P4, 274 more genes
    nsv3912429copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,800,931-95,730,598 , NCBI36 chr4: 82,019,955-95,949,621 , GRCh38 chr4: 80,879,777-94,809,447 CFAP299, RNU6-469P, 152 more genes
    nsv4674589copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079 CFAP299, SOWAHB, 211 more genes
    nsv6291249copy number variation1nstd102humanPathogenic GRCh37 chr4: 80,467,886-93,362,064 , GRCh38.p12 chr4: 79,546,732-92,440,913 CFAP299, HNRNPA3P13, 155 more genes
    nsv3916835copy number variation1nstd102humanPathogenic GRCh37 chr4: 80,496,902-93,333,600 , GRCh38 chr4: 79,575,748-92,412,449 , NCBI36 chr4: 80,715,926-93,552,623 CFAP299, SLC10A6, 155 more genes
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