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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7088732copy number variation1nstd229human GRCh38 chrX: 72,044,201-72,049,500 , GRCh37.p13 chrX: 71,264,051-71,269,350 RPS26P11, NHSL2
    esv3239831copy number variation1estd209human GRCh37 chrX: 71,262,604-71,262,606 , GRCh38.p12 chrX: 72,042,754-72,042,756 RPS26P11, NHSL2
    esv2121426copy number variation1estd194human NCBI36 chrX: 71,179,330-71,179,332 , GRCh37.p13 chrX: 71,262,605-71,262,607 , GRCh38.p12 chrX: 72,042,755-72,042,757 NHSL2, RPS26P11
    esv1093653copy number variation1estd22human NCBI36 chrX: 71,179,342-71,179,344 , GRCh37.p13 chrX: 71,262,617-71,262,619 , GRCh38.p12 chrX: 72,042,767-72,042,769 RPS26P11, NHSL2
    nsv425877copy number variation1nstd6human NCBI35 chrX: 71,045,639-71,045,640 , GRCh37.p13 chrX: 71,262,618-71,262,619 , GRCh38.p12 chrX: 72,042,768-72,042,769 NHSL2, RPS26P11
    nsv421218copy number variation1nstd6human NCBI35 chrX: 71,045,626-71,045,627 , GRCh37.p13 chrX: 71,262,605-71,262,606 , GRCh38.p12 chrX: 72,042,755-72,042,756 NHSL2, RPS26P11
    nsv7032220inversion1nstd229human GRCh38 chrX: 72,044,644-72,045,402 , GRCh37.p13 chrX: 71,264,494-71,265,252 RPS26P11, NHSL2
    nsv2695478short tandem repeat5nstd128human GRCh37 chrX: 71,262,605-71,262,619 , GRCh38.p12 chrX: 72,042,755-72,042,769 NHSL2, RPS26P11
    nsv2676045short tandem repeat3nstd128human GRCh37 chrX: 71,264,810-71,264,824 , GRCh38.p12 chrX: 72,044,960-72,044,974 NHSL2, RPS26P11
    nsv7088724copy number variation1nstd229human GRCh38 chrX: 71,941,829-72,060,461 , GRCh37.p13 chrX: 71,161,679-71,280,311 RPS26P11, RNU6-1078P, 1 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 NANOGNBP3, PRXL2CP1, 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 NHS-AS1, DUSP21, 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 GPR119, RN7SKP81, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 H2AB2, RTL3, 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 OR3B1P, SSX4B, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 ARMCX2, RNA5SP505, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 NDUFB11, VN1R110P, 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 SLC38A5, CT45A1, 2152 more genes
    nsv3885865copy number variation1nstd102humanPathogenic GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920 MIR1277, LOC100420247, 2152 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
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