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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6291828insertion1nstd102humanBenign GRCh38 chr22: 19,919,729-19,919,729 , GRCh37 chr22: 19,907,252-19,907,252 TXNRD2
    nsv3877704copy number variation1nstd102humanUncertain significance GRCh38 chr22: 19,911,357-19,911,467 , GRCh37 chr22: 19,898,880-19,898,990 TXNRD2
    nsv4682566copy number variation1nstd102humanUncertain significance GRCh37 chr22: 19,898,890-19,898,980 , GRCh38.p12 chr22: 19,911,367-19,911,457 TXNRD2
    nsv7096292copy number variation1nstd102humanUncertain significance GRCh37 chr22: 19,864,628-19,883,124 , GRCh38.p12 chr22: 19,877,105-19,895,601 TXNRD2, RPL8P5
    nsv3878411copy number variation1nstd102humanUncertain significance GRCh37 chr22: 19,918,533-19,929,346 , GRCh38 chr22: 19,931,010-19,941,823 TXNRD2, COMT
    nsv4457393copy number variation1nstd102humanUncertain significance GRCh37 chr22: 19,905,801-19,938,011 , GRCh38.p12 chr22: 19,918,278-19,950,488 TXNRD2, COMT
    nsv6311119copy number variation1nstd102humanUncertain significance GRCh37 chr22: 19,929,214-19,929,336 , GRCh38.p12 chr22: 19,941,691-19,941,813 TXNRD2, COMT
    nsv4681469copy number variation1nstd102humanUncertain significance GRCh37 chr22: 19,864,618-19,929,336 , GRCh38.p12 chr22: 19,877,095-19,941,813 TXNRD2, RPL8P5, 1 more genes
    nsv6311315copy number variation1nstd102humanUncertain significance GRCh37 chr22: 19,918,553-19,969,614 , GRCh38.p12 chr22: 19,931,030-19,982,091 TXNRD2, ARVCF, 2 more genes
    nsv6311176copy number variation1nstd102humanUncertain significance GRCh37 chr22: 19,862,041-19,930,515 , GRCh38.p12 chr22: 19,874,518-19,942,992 TXNRD2, COMT, 1 more genes
    nsv4451067copy number variation1nstd102humanUncertain significance GRCh37 chr22: 19,864,618-19,929,336 , GRCh38 chr22: 19,877,095-19,941,813 TXNRD2, RPL8P5, 1 more genes
    nsv4674327copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,475,385-23,764,120 , GRCh38.p12 chr22: 17,992,619-23,421,933 TXNRD2, GP1BB, 308 more genes
    nsv3917936copy number variation1nstd102humanPathogenic NCBI36 chr22: 18,659,766-22,152,986 , GRCh38 chr22: 18,339,130-23,480,799 , GRCh37 chr22: 20,279,766-23,822,986 TXNRD2, IGLV7-46, 298 more genes
    nsv4676119copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-20,730,144 , GRCh38.p12 chr22: 16,408,173-20,375,854 TXNRD2, C22orf39, 150 more genes
    nsv3923978copy number variation1nstd102humanPathogenic NCBI36 chr22: 15,399,015-19,048,227 , GRCh37 chr22: 17,019,015-20,718,227 , GRCh38 chr22: 16,538,125-20,363,937 TXNRD2, MIR185, 146 more genes
    nsv4676296copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-20,125,005 , GRCh38.p12 chr22: 16,408,173-20,137,482 TXNRD2, FAM230J, 139 more genes
    nsv3895935copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,900-20,026,751 , GRCh38.p12 chr22: 16,408,174-20,039,228 TXNRD2, FAM247C, 131 more genes
    nsv3913197copy number variation2nstd102humanPathogenic GRCh37 chr22: 17,397,498-20,708,934 , GRCh38 chr22: 16,916,608-20,354,644 , NCBI36 chr22: 15,777,498-19,038,934 TXNRD2, E2F6P1, 128 more genes
    nsv3910919copy number variation2nstd102humanPathogenic NCBI36 chr22: 15,777,498-18,691,763 , GRCh37 chr22: 17,397,498-20,311,763 , GRCh38 chr22: 16,916,608-20,324,240 TXNRD2, C22orf39, 127 more genes
    nsv3901351copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,644,790-21,915,509 , GRCh38.p12 chr22: 18,162,023-21,561,220 TXNRD2, RPL34P35, 149 more genes
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