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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381485copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 12,693,997-12,702,458 , GRCh38.p12 chr9: 12,693,997-12,702,458 TYRP1, LURAP1L-AS1
    nsv3924823copy number variation1nstd102humanUncertain significance NCBI36 chr9: 12,439,564-12,729,192 , GRCh37 chr9: 12,449,564-12,739,192 , GRCh38 chr9: 12,449,564-12,739,193 TYRP1, LURAP1L-AS1
    nsv4455161copy number variation1nstd102humanUncertain significance GRCh37 chr9: 12,552,814-12,700,251 , GRCh38.p12 chr9: 12,552,814-12,700,251 TYRP1, LURAP1L-AS1
    nsv4676077copy number variation1nstd102humanUncertain significance GRCh37 chr9: 12,687,248-12,761,919 , GRCh38.p12 chr9: 12,687,248-12,761,920 TYRP1, LURAP1L-AS1
    nsv6313247copy number variation1nstd102humanUncertain significance GRCh37 chr9: 12,709,144-12,712,827 , GRCh38.p12 chr9: 12,709,144-12,712,828 TYRP1, LURAP1L-AS1
    nsv7097923copy number variation1nstd102humanUncertain significance GRCh37 chr9: 12,693,997-12,709,182 , GRCh38.p12 chr9: 12,693,997-12,709,182 TYRP1, LURAP1L-AS1
    nsv3894632copy number variation1nstd102humanBenign GRCh37 chr9: 12,628,213-12,861,280 , GRCh38.p12 chr9: 12,628,213-12,861,281 TYRP1, LURAP1L-AS1, 2 more genes
    nsv3908599copy number variation1nstd102humanLikely benign GRCh37 chr9: 12,643,510-12,794,563 , GRCh38.p12 chr9: 12,643,510-12,794,564 TYRP1, LURAP1L, 2 more genes
    nsv3907958copy number variation1nstd102humanLikely benign GRCh37 chr9: 12,113,524-12,739,192 , GRCh38.p12 chr9: 12,113,524-12,739,193 TYRP1, LURAP1L-AS1, 3 more genes
    nsv3920950copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,104-18,872,279 , GRCh37 chr9: 204,104-18,882,279 , GRCh38 chr9: 204,104-18,882,281 TYRP1, RPL4P5, 193 more genes
    nsv3910019copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,708,805 , NCBI36 chr9: 210,253-18,698,803 , GRCh37 chr9: 220,253-18,708,803 TYRP1, LOC107987049, 191 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 TYRP1, ACTG1P14, 191 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 TYRP1, DOCK8-AS1, 186 more genes
    nsv3910119copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,193-18,063,357 , GRCh38 chr9: 204,193-18,073,359 , GRCh37 chr9: 204,193-18,073,357 TYRP1, RNA5SP279, 186 more genes
    nsv3917303copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,073,359 , GRCh37 chr9: 220,253-18,073,357 , NCBI36 chr9: 210,253-18,063,357 TYRP1, DMAC1, 185 more genes
    nsv4674929copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412 TYRP1, LINC02851, 184 more genes
    nsv3905168copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,655,298 , GRCh38.p12 chr9: 203,861-17,655,300 TYRP1, RANBP6, 184 more genes
    nsv3899178copy number variation1nstd102humanPathogenic GRCh37 chr9: 213,161-17,496,750 , GRCh38.p12 chr9: 213,161-17,496,752 TYRP1, GLIS3, 181 more genes
    nsv3903505copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,125,893 , GRCh38.p12 chr9: 203,861-17,125,895 TYRP1, RPS26P3, 179 more genes
    nsv3923785copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,193-16,887,578 , GRCh37 chr9: 204,193-16,897,578 , GRCh38 chr9: 204,193-16,897,580 TYRP1, FTH1P12, 176 more genes
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