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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4451375copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,395,893-154,449,928 , GRCh38.p12 chrX: 155,167,618-155,221,651 VBP1
    nsv3882292copy number variation1nstd102humanBenign GRCh37 chrX: 154,305,616-154,440,581 , GRCh38.p12 chrX: 155,077,341-155,212,303 VBP1, BRCC3
    nsv4452822copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,301,825-154,443,920 , GRCh38.p12 chrX: 155,073,550-155,215,643 VBP1, BRCC3
    nsv4450446copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,301,825-154,443,882 , GRCh38.p12 chrX: 155,073,550-155,215,605 VBP1, BRCC3
    nsv4673923copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 154,418,280-154,565,718 , GRCh38.p12 chrX: 155,190,005-155,336,409 VBP1, CLIC2, 3 more genes
    nsv6290459copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,289,110-154,447,538 , GRCh38.p12 chrX: 155,060,835-155,219,261 VBP1, BRCC3, 2 more genes
    nsv4728325copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,290,230-154,441,876 , GRCh38.p12 chrX: 155,061,955-155,213,598 VBP1, MTCP1, 2 more genes
    nsv6290588copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,296,576-154,447,527 , GRCh38.p12 chrX: 155,068,301-155,219,250 VBP1, MTCP1, 2 more genes
    nsv6636710copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,296,580-154,447,527 , GRCh38.p12 chrX: 155,068,305-155,219,250 VBP1, MTCP1, 2 more genes
    nsv3879713copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,296,581-154,443,920 , GRCh38.p12 chrX: 155,068,306-155,215,643 VBP1, BRCC3, 2 more genes
    nsv6636378copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,296,582-154,441,876 , GRCh38.p12 chrX: 155,068,307-155,213,598 VBP1, MTCP1, 2 more genes
    nsv3905035copy number variation1nstd102humanUncertain significance NCBI36 chrX: 154,108,685-154,213,569 , GRCh38 chrX: 155,227,210-155,331,063 , GRCh37 chrX: 154,455,491-154,560,375 VBP1, TWF1P2, 3 more genes
    nsv3904162copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754 VBP1, NANOGNBP3, 2154 more genes
    nsv3913255copy number variation2nstd102humanPathogenic NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895 VBP1, NHS-AS1, 2154 more genes
    nsv3907094copy number variation4nstd102humanPathogenic GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065 VBP1, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 VBP1, H2AB2, 2152 more genes
    nsv3898149copy number variation1nstd102humanPathogenic GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792 VBP1, OR3B1P, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 VBP1, ARMCX2, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 VBP1, NDUFB11, 2154 more genes
    nsv3903061copy number variation1nstd102humanPathogenic NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832 VBP1, SLC38A5, 2152 more genes
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