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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6638046copy number variation1nstd102humanUncertain significance GRCh37 chr9: 15,241,646-15,504,917 , GRCh38.p12 chr9: 15,241,648-15,504,919 PSIP1, TTC39B, 3 more genes
    nsv4675845copy number variation1nstd102humanUncertain significance GRCh37 chr9: 15,241,645-15,504,916 , GRCh38.p12 chr9: 15,241,647-15,504,918 PSIP1, TTC39B, 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 PSIP1, 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 PSIP1, LOC107987049, 191 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 PSIP1, ACTG1P14, 191 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 PSIP1, 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 PSIP1, 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 PSIP1, DMAC1, 185 more genes
    nsv4674929copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412 PSIP1, LINC02851, 184 more genes
    nsv3905168copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,655,298 , GRCh38.p12 chr9: 203,861-17,655,300 PSIP1, RANBP6, 184 more genes
    nsv3899178copy number variation1nstd102humanPathogenic GRCh37 chr9: 213,161-17,496,750 , GRCh38.p12 chr9: 213,161-17,496,752 PSIP1, GLIS3, 181 more genes
    nsv3903505copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,125,893 , GRCh38.p12 chr9: 203,861-17,125,895 PSIP1, 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 PSIP1, FTH1P12, 176 more genes
    nsv3890932copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-16,856,907 , GRCh38.p12 chr9: 203,861-16,856,909 PSIP1, ACTG1P14, 176 more genes
    nsv3917732copy number variation1nstd102humanPathogenic GRCh38 chr9: 214,367-16,307,944 , GRCh37 chr9: 214,367-16,307,942 , NCBI36 chr9: 204,367-16,297,942 PSIP1, RLN1, 173 more genes
    nsv3919683copy number variation1nstd102humanPathogenic GRCh38 chr9: 322,690-16,401,656 , NCBI36 chr9: 312,690-16,391,654 , GRCh37 chr9: 322,690-16,401,654 PSIP1, DMRT2, 172 more genes
    nsv6315395copy number variation1nstd102humanPathogenic GRCh37 chr9: 4,992,582-19,322,101 , GRCh38.p12 chr9: 4,992,582-19,322,103 PSIP1, FREM1, 142 more genes
    nsv3921658copy number variation1nstd102humanPathogenic GRCh38 chr9: 9,661,633-18,034,356 , GRCh37 chr9: 9,661,633-18,034,354 , NCBI36 chr9: 9,651,633-18,024,354 PSIP1, LURAP1L, 67 more genes
    nsv3914995copy number variation1nstd102humanPathogenic GRCh37 chr9: 11,086,096-17,636,669 , NCBI36 chr9: 11,076,096-17,626,669 , GRCh38 chr9: 11,086,096-17,636,671 PSIP1, CLCN3P1, 60 more genes
    nsv3911366copy number variation1nstd102humanPathogenic GRCh37 chr9: 11,818,291-17,963,880 , GRCh38 chr9: 11,818,291-17,963,882 , NCBI36 chr9: 11,808,291-17,953,880 PSIP1, RN7SL98P, 59 more genes
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