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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097211copy number variation1nstd102humanUncertain significance GRCh37 chr3: 58,419,338-58,419,536 , GRCh38.p12 chr3: 58,433,611-58,433,809 PDHB
    nsv7097210copy number variation1nstd102humanUncertain significance GRCh37 chr3: 57,130,421-58,520,833 , GRCh38.p12 chr3: 57,096,393-58,535,106 LOC107984079, SLMAP, 37 more genes
    nsv7051968inversion1nstd229human GRCh38 chr3: 56,944,702-65,952,705 , GRCh37.p13 chr3: 56,978,730-65,938,380 ILF2P1, ARHGEF3-AS1, 115 more genes
    nsv7050374inversion1nstd229human GRCh38 chr3: 58,433,663-58,433,765 , GRCh37.p13 chr3: 58,419,390-58,419,492 PDHB
    nsv7042731inversion1nstd229human GRCh38 chr3: 57,478,691-59,225,228 , GRCh37.p13 chr3: 57,464,418-59,210,954 ARF4-AS1, RNF7P1, 37 more genes
    nsv6709666copy number variation1nstd229human GRCh38 chr3: 58,425,416-58,428,350 , GRCh37.p13 chr3: 58,411,143-58,414,077 PDHB, PXK
    nsv6373326copy number variation1nstd223human GRCh38 chr3: 58,425,416-58,428,347 , GRCh37.p13 chr3: 58,411,143-58,414,074 PDHB, PXK
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4452524copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281 LOC105377114, FAM107A, 110 more genes
    nsv4450673copy number variation1nstd102humanUncertain significance GRCh38 chr3: 58,428,014-58,431,813 , GRCh37 chr3: 58,413,741-58,417,540 PDHB
    nsv4073311copy number variation1nstd166human GRCh37.p13 chr3: 58,417,830-58,419,319 , GRCh38.p12 chr3: 58,432,103-58,433,592 PDHB
    nsv3919181copy number variation1nstd102humanPathogenic GRCh38 chr3: 54,045,018-66,060,461 , GRCh37 chr3: 54,079,045-66,046,136 , NCBI36 chr3: 54,054,085-66,021,176 MAGI1-AS1, FEZF2, 135 more genes
    nsv3917204copy number variation1nstd102humanPathogenic GRCh38 chr3: 57,430,538-64,884,522 , NCBI36 chr3: 57,391,305-64,845,237 , GRCh37 chr3: 57,416,265-64,870,197 C3orf49, PPIAP16, 93 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 LOC105377171, HNRNPA3P6, 323 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3886371copy number variation1nstd102humanBenign GRCh37 chr3: 58,089,516-58,799,748 , GRCh38.p12 chr3: 58,103,789-58,814,022 ACOX2, ABHD6, 18 more genes
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