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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv997095copy number variation1nstd45humanPathogenic GRCh37 chrX: 15,843,929-15,873,137 , GRCh38.p12 chrX: 15,825,806-15,855,014 ZRSR2, AP1S2
    nsv3877977copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,172,610-112,244,011 , GRCh38 chr5: 112,836,913-112,908,314 REEP5, XBP1P1, 3 more genes
    nsv6636037copy number variation1nstd102humanPathogenic GRCh38 chr5: 112,837,231-112,890,913 , GRCh37.p13 chr5: 112,172,928-112,226,610 ZRSR2P1, REEP5, 3 more genes
    nsv3874322copy number variation1nstd102humanBenign GRCh37 chr5: 112,196,949-112,252,066 , GRCh38.p12 chr5: 112,861,252-112,916,369 XBP1P1, SRP19, 2 more genes
    nsv4675389copy number variation1nstd102humanUncertain significance GRCh37 chr5: 112,206,135-112,272,761 , GRCh38.p12 chr5: 112,870,438-112,937,064 ZRSR2P1, REEP5, 3 more genes
    nsv6312167copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,173,731-112,343,239 , GRCh38.p12 chr5: 112,838,034-113,007,542 APC, SRP19, 6 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 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
    nsv3907545copy number variation1nstd102humanPathogenic GRCh37 chrX: 64,245-155,228,958 , NCBI36 chrX: 4,245-154,882,152 , GRCh38 chrX: 14,245-155,999,293 TMEM30BP1, SPANXB1, 2151 more genes
    nsv3884029copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,224,766 , GRCh38.p12 chrX: 21,267-155,995,101 SSX4B, LOC100420083, 2150 more genes
    nsv3898185copy number variation2nstd102humanPathogenic GRCh37 chrX: 76,102-155,226,096 , NCBI36 chrX: 16,102-154,879,290 , GRCh38 chrX: 26,102-155,996,431 ANKRD11P2, RAI2, 2151 more genes
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