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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3884692copy number variation1nstd102humanBenign GRCh37 chrX: 46,408,015-46,434,557 , GRCh38.p12 chrX: 46,548,580-46,575,122 CHST7, ZNF674-AS1, 1 more genes
    nsv3892302copy number variation1nstd102humanBenign GRCh38 chrX: 46,548,195-46,673,443 , NCBI36 chrX: 46,292,574-46,417,822 , GRCh37 chrX: 46,407,630-46,532,878 MKI67P1, CHST7, 3 more genes
    nsv3877132copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,366,112-46,407,917 , GRCh38.p12 chrX: 46,506,677-46,548,482 ZNF674, ZNF674-AS1, 1 more genes
    nsv3881944copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,366,112-46,407,858 , GRCh38.p12 chrX: 46,506,677-46,548,423 ZNF674, RNU6-50P, 1 more genes
    nsv3906983copy number variation1nstd102humanUncertain significance NCBI36 chrX: 46,252,456-46,292,861 , GRCh37 chrX: 46,367,512-46,407,917 , GRCh38 chrX: 46,508,077-46,548,482 ZNF674, RNU6-50P, 1 more genes
    nsv4450752copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,371,061-46,408,859 , GRCh38.p12 chrX: 46,511,626-46,549,424 ZNF674, ZNF674-AS1, 1 more genes
    nsv4449829copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,371,061-46,408,674 , GRCh38.p12 chrX: 46,511,626-46,549,239 ZNF674, ZNF674-AS1, 1 more genes
    nsv4450574copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,371,128-46,408,674 , GRCh38.p12 chrX: 46,511,693-46,549,239 ZNF674, ZNF674-AS1, 1 more genes
    nsv3890250copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,392,023-46,427,876 , GRCh38 chrX: 46,532,588-46,568,441 , NCBI36 chrX: 46,276,967-46,312,820 ZNF674, MKI67P1, 1 more genes
    nsv3890069copy number variation1nstd102humanUncertain significance NCBI36 chrX: 46,258,472-46,292,861 , GRCh37 chrX: 46,373,528-46,407,917 , GRCh38 chrX: 46,514,093-46,548,482 ZNF674, RNU6-50P, 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 ZNF674, 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 ZNF674, 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 ZNF674, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 ZNF674, 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 ZNF674, OR3B1P, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 ZNF674, ARMCX2, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 ZNF674, 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 ZNF674, SLC38A5, 2152 more genes
    nsv3885865copy number variation1nstd102humanPathogenic GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920 ZNF674, MIR1277, 2152 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 ZNF674, LOC105373176, 2151 more genes
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