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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905064copy number variation1nstd102humanBenign GRCh37 chr9: 4,600,001-4,600,420 , GRCh38.p12 chr9: 4,600,001-4,600,420 SPATA6L
    nsv3905189copy number variation1nstd102humanBenign GRCh37 chr9: 4,600,001-4,600,401 , GRCh38.p12 chr9: 4,600,001-4,600,401 SPATA6L
    nsv3892415copy number variation1nstd102humanBenign GRCh37 chr9: 4,600,001-4,600,368 , GRCh38.p12 chr9: 4,600,001-4,600,368 SPATA6L
    nsv3894912copy number variation1nstd102humanBenign GRCh37 chr9: 4,600,001-4,600,301 , GRCh38.p12 chr9: 4,600,001-4,600,301 SPATA6L
    nsv3895953copy number variation1nstd102humanBenign GRCh37 chr9: 4,600,001-4,600,237 , GRCh38.p12 chr9: 4,600,001-4,600,237 SPATA6L
    nsv3904696copy number variation1nstd102humanBenign GRCh37 chr9: 4,600,001-4,600,201 , GRCh38.p12 chr9: 4,600,001-4,600,201 SPATA6L
    nsv6291048copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,493,035-4,620,791 , GRCh38.p12 chr9: 4,493,035-4,620,791 SPATA6L, SLC1A1
    nsv6291296copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,128,010-4,547,288 , GRCh38.p12 chr9: 4,128,010-4,547,288 SPATA6L, SLC1A1, 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 SPATA6L, 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 SPATA6L, LOC107987049, 191 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 SPATA6L, ACTG1P14, 191 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 SPATA6L, 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 SPATA6L, 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 SPATA6L, DMAC1, 185 more genes
    nsv4674929copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412 SPATA6L, LINC02851, 184 more genes
    nsv3905168copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,655,298 , GRCh38.p12 chr9: 203,861-17,655,300 SPATA6L, RANBP6, 184 more genes
    nsv3899178copy number variation1nstd102humanPathogenic GRCh37 chr9: 213,161-17,496,750 , GRCh38.p12 chr9: 213,161-17,496,752 SPATA6L, GLIS3, 181 more genes
    nsv3903505copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,125,893 , GRCh38.p12 chr9: 203,861-17,125,895 SPATA6L, 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 SPATA6L, FTH1P12, 176 more genes
    nsv3890932copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-16,856,907 , GRCh38.p12 chr9: 203,861-16,856,909 SPATA6L, ACTG1P14, 176 more genes
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