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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 FAM102A, LOC107987132, 51 more genes
    nsv4985740copy number variation1nstd200human GRCh38 chr9: 128,105,845-128,709,294 , GRCh37.p13 chr9: 130,868,124-131,471,573 MIR199B, SET, 33 more genes
    nsv4983738copy number variation1nstd200human GRCh38 chr9: 128,155,449-128,158,935 , GRCh37.p13 chr9: 130,917,728-130,921,214 BBLN
    nsv4768374copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685 SPTAN1, NAIF1, 54 more genes
    nsv4683557copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,577,951-131,303,459 , GRCh38.p12 chr9: 127,815,672-128,541,180 LOC105376286, SWI5, 36 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 IFNA14, NUP188, 2233 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 PLPPR1, TPT1P9, 1341 more genes
    nsv4450425copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 130,374,663-131,329,276 , GRCh38 chr9: 127,612,384-128,566,997 FAM102A, ST6GALNAC6, 50 more genes
    nsv4450184copy number variation1nstd102humanUncertain significance GRCh37 chr9: 130,216,797-130,953,151 , GRCh38 chr9: 127,454,518-128,190,872 MIR3911, LOC107987132, 32 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABL1, 927 more genes
    nsv4180801copy number variation1nstd166human GRCh37.p13 chr9: 130,923,251-130,924,117 , GRCh38.p12 chr9: 128,160,972-128,161,838 BBLN
    nsv3924370copy number variation1nstd102humanPathogenic NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225 LOC102723566, MIR2861, 101 more genes
    nsv3923672copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,681,755-132,842,253 , GRCh38 chr9: 127,919,476-130,079,974 , NCBI36 chr9: 129,721,576-131,882,074 TBC1D13, LINC01503, 81 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 TUBBP4, MOB3B, 2236 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 LOC105375956, TUBBP4, 2233 more genes
    nsv3920829copy number variation1nstd102humanPathogenic GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497 DAB2IP, SOHLH1, 506 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 EIF4A1P3, MVB12B, 2233 more genes
    nsv3919948copy number variation1nstd102humanPathogenic GRCh37 chr9: 125,554,937-141,018,984 , GRCh38 chr9: 122,792,658-138,124,532 , NCBI36 chr9: 124,594,758-140,138,805 LCNL1, C9orf116, 467 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 RPL23AP57, RPL35AP20, 2235 more genes
    nsv3918439copy number variation1nstd102humanPathogenic GRCh38 chr9: 121,073,102-138,179,445 , GRCh37 chr9: 123,835,380-141,073,897 , NCBI36 chr9: 122,875,201-140,193,718 LRRC26, ASB6, 509 more genes
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