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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5476949copy number variation1nstd206human GRCh37.p13 chr9|NW_003871067.1: 215,000-295,379 , GRCh38 chr9: 68,435,552-68,584,552 , GRCh37.p13 chr9: 71,050,468-71,130,847 LINC01506, TMEM252-DT, 2 more genes
    nsv4526449copy number variation1nstd166human GRCh37.p13 chr9: 71,108,999-71,379,000 , GRCh38.p12 chr9: 68,494,083-68,764,084 PGM5, PIP5K1B, 5 more genes
    nsv4481893mobile element insertion1nstd166human GRCh37.p13 chr9: 71,158,876-71,158,876 , GRCh38.p12 chr9: 68,543,960-68,543,960 TMEM252-DT, LINC01506
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 RPL35AP21, LOC105376097, 134 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv4421062copy number variation1nstd174human GRCh37 chr9: 71,009,095-71,200,407 , GRCh38.p12 chr9: 68,394,179-68,585,491 LINC01506, PGM5, 3 more genes
    nsv4371052copy number variation3nstd173human GRCh37 chr9: 71,050,682-71,196,279 , GRCh38.p12 chr9: 68,435,766-68,581,363 LINC01506, TMEM252, 2 more genes
    nsv4178799copy number variation1nstd166human GRCh37.p13 chr9: 71,109,000-71,199,000 , GRCh38.p12 chr9: 68,494,084-68,584,084 TMEM252-DT, PGM5, 2 more genes
    nsv3923714copy number variation1nstd102humanPathogenic GRCh38 chr9: 193,412-70,630,731 , GRCh37 chr9: 220,253-73,245,647 , NCBI36 chr9: 210,253-72,435,467 LOC105379257, LOC105376002, 888 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3921582copy number variation1nstd102humanPathogenic GRCh38 chr9: 68,426,796-69,606,104 , NCBI36 chr9: 70,231,532-71,410,840 , GRCh37 chr9: 71,130,848-72,221,020 LOC105376071, PRKACG, 15 more genes
    nsv3920777copy number variation1nstd102humanPathogenic NCBI36 chr9: 70,259,583-78,057,599 , GRCh38 chr9: 68,454,847-76,252,863 , GRCh37 chr9: 71,130,848-78,867,779 ANXA1, LOC105376080, 96 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
    nsv3919257copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718 LOC107987031, LOC105376234, 2169 more genes
    nsv3917022copy number variation1nstd102humanPathogenic GRCh37 chr9: 214,367-141,008,915 , GRCh38 chr9: 193,412-138,114,463 , NCBI36 chr9: 204,367-140,128,736 RN7SKP87, SPATA6L, 2168 more genes
    nsv3915973copy number variation2nstd102humanPathogenic GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346 CTNNAL1, QSOX2, 2170 more genes
    nsv3915174copy number variation1nstd102humanPathogenic NCBI36 chr9: 70,304,266-85,474,962 , GRCh38 chr9: 68,499,530-83,670,227 , GRCh37 chr9: 71,130,848-86,285,142 LOC107987086, PGM5, 183 more genes
    nsv3915095copy number variation1nstd102humanPathogenic GRCh38 chr9: 193,412-74,615,913 , NCBI36 chr9: 194,193-76,420,649 , GRCh37 chr9: 204,193-77,230,829 MTCO3P36, BMS1P14, 934 more genes
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