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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4453070copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,109,551-24,110,169 , GRCh38 chr22: 23,767,364-23,767,982 CHCHD10, LOC107985577
    nsv5381316copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,109,541-24,110,081 , GRCh38.p12 chr22: 23,767,354-23,767,894 , GRCh38.p12 chr22|NT_187633.1: 3,716-4,256 CHCHD10, LOC107985577
    nsv7095931copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,109,541-24,110,061 , GRCh38.p12 chr22: 23,767,354-23,767,874 , GRCh38.p12 chr22|NT_187633.1: 3,716-4,236 CHCHD10, LOC107985577
    nsv5033431copy number variation1nstd200human GRCh38 chr22: 23,766,424-23,767,270 , GRCh37.p13 chr22: 24,108,611-24,109,457 CHCHD10, LOC107985577
    nsv4869186copy number variation1nstd200human GRCh37 chr22: 24,108,611-24,109,457 , GRCh38.p12 chr22: 23,766,424-23,767,270 , GRCh38.p12 chr22|NT_187633.1: 2,786-3,632 CHCHD10, LOC107985577
    esv1354053copy number variation1estd22human NCBI36 chr22: 22,438,656-22,438,657 , GRCh37.p13 chr22: 24,108,656-24,108,657 , GRCh38.p12 chr22|NT_187633.1: 2,831-2,832 , GRCh38.p12 chr22: 23,766,469-23,766,470 CHCHD10, LOC107985577
    nsv4681263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,108,011-24,109,790 , GRCh38.p12 chr22: 23,765,824-23,767,603 , GRCh38.p12 chr22|NT_187633.1: 2,186-3,965 CHCHD10, LOC107985577, 1 more genes
    nsv7096341copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,108,194-24,108,482 , GRCh38.p12 chr22|NT_187633.1: 2,369-2,657 , GRCh38.p12 chr22: 23,766,007-23,766,295 CHCHD10, LOC107985577, 1 more genes
    nsv4452836copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,108,011-24,110,169 , GRCh38 chr22: 23,765,824-23,767,982 CHCHD10, LOC107985577, 1 more genes
    nsv3888358copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,108,174-24,110,081 , GRCh38 chr22: 23,765,987-23,767,894 CHCHD10, LOC107985577, 1 more genes
    nsv7025513copy number variation1nstd229human GRCh38 chr22: 23,766,751-23,771,766 , GRCh37.p13 chr22: 24,108,938-24,113,953 CHCHD10, MMP11, 1 more genes
    nsv7019205copy number variation1nstd229human GRCh38 chr22: 23,765,543-23,766,328 , GRCh37.p13 chr22: 24,107,730-24,108,515 CHCHD10, LOC107985577, 1 more genes
    nsv6545899copy number variation1nstd223human GRCh38 chr22: 23,766,738-23,771,765 , GRCh37.p13 chr22: 24,108,925-24,113,952 CHCHD10, LOC107985577, 1 more genes
    nsv5033192copy number variation1nstd200human GRCh38 chr22: 23,765,574-23,767,297 , GRCh37.p13 chr22: 24,107,761-24,109,484 CHCHD10, LOC107985577, 1 more genes
    nsv4869185copy number variation1nstd200human GRCh37 chr22: 24,107,790-24,109,457 , GRCh38.p12 chr22|NT_187633.1: 1,965-3,632 , GRCh38.p12 chr22: 23,765,603-23,767,270 CHCHD10, C22orf15, 1 more genes
    nsv5031862copy number variation1nstd200human GRCh38 chr22: 23,765,605-23,766,344 , GRCh37.p13 chr22: 24,107,792-24,108,531 CHCHD10, C22orf15, 1 more genes
    nsv4869184copy number variation1nstd200human GRCh37 chr22: 24,107,792-24,108,531 , GRCh38.p12 chr22: 23,765,605-23,766,344 , GRCh38.p12 chr22|NT_187633.1: 1,967-2,706 CHCHD10, LOC107985577, 1 more genes
    nsv4282536copy number variation1nstd166human GRCh37.p13 chr22: 24,108,926-24,113,952 , GRCh38.p12 chr22|NT_187633.1: 3,101-8,127 , GRCh38.p12 chr22: 23,766,739-23,771,765 CHCHD10, MMP11, 1 more genes
    nsv5365769translocation1nstd200human GRCh38 chr17: 42,410,299-42,410,299 , GRCh38 chr22: 23,767,606-23,767,606 , GRCh37.p13 chr17: 40,562,317-40,562,317 , GRCh37.p13 chr22: 24,109,793-24,109,793 CHCHD10, CAVIN1, 1 more genes
    nsv5334048translocation1nstd200human GRCh37 chr17: 40,562,317-40,562,317 , GRCh37 chr22: 24,109,793-24,109,793 , GRCh38.p12 chr17: 42,410,299-42,410,299 , GRCh38.p12 chr22: 23,767,606-23,767,606 , GRCh38.p12 chr22|NT_187633.1: 3,968-3,968 CHCHD10, CAVIN1, 1 more genes
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