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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3891322copy number variation2nstd102humanPathogenic NCBI36 chrX: 153,865,975-153,979,913 , GRCh37.p13 chrX|NW_003871103.3: 2,418,485-2,532,423 , GRCh38 chrX: 154,984,506-155,098,444 CMC4, BRCC3, 3 more genes
    nsv3881029copy number variation1nstd102humanPathogenic GRCh37 chrX: 154,250,433-154,317,840 , GRCh38.p12 chrX: 155,022,158-155,089,565 CMC4, F8, 3 more genes
    nsv4674664copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 154,252,722-154,343,784 , GRCh38.p12 chrX: 155,024,447-155,115,509 CMC4, MTCP1, 2 more genes
    nsv3874110copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 154,256,858-154,297,348 , GRCh38.p12 chrX: 155,028,583-155,069,073 CMC4, MTCP1, 1 more genes
    nsv7093362copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,261,678-154,305,564 , GRCh38.p12 chrX: 155,033,403-155,077,289 CMC4, FUNDC2, 2 more genes
    nsv5059975copy number variation1nstd102humanUncertain significance GRCh38 chrX: 155,049,151-155,071,205 , GRCh37 chrX: 154,277,426-154,299,480 CMC4, BRCC3, 2 more genes
    nsv6290459copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,289,110-154,447,538 , GRCh38.p12 chrX: 155,060,835-155,219,261 CMC4, 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 CMC4, 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 CMC4, 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 CMC4, 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 CMC4, VBP1, 2 more genes
    nsv6636378copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,296,582-154,441,876 , GRCh38.p12 chrX: 155,068,307-155,213,598 CMC4, MTCP1, 2 more genes
    nsv4451627copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,238,385-154,339,708 , GRCh38.p12 chrX: 155,010,110-155,111,433 CMC4, MTCP1, 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 CMC4, 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 CMC4, 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 CMC4, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 CMC4, 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 CMC4, OR3B1P, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 CMC4, ARMCX2, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 CMC4, NDUFB11, 2154 more genes
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