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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5674178copy number variation1nstd102humanPathogenic GRCh37 chr9: 98,204,264-98,271,831 , GRCh38.p12 chr9: 95,441,982-95,509,549 PTCH1, LOC100507346
    nsv5673897copy number variation1nstd102humanPathogenic GRCh37 chr9: 98,229,392-98,232,219 , GRCh38.p12 chr9: 95,467,110-95,469,937 LOC100507346, PTCH1
    nsv5564503copy number variation1nstd102humanUncertain significance GRCh37 chr9: 98,226,337-98,248,166 , GRCh38.p12 chr9: 95,464,055-95,485,884 PTCH1, LOC100507346
    nsv5381709copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 97,863,989-98,279,100 , GRCh38.p12 chr9: 95,101,707-95,516,818 RPS26P37, LOC105376155, 9 more genes
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 ALDOB, CAVIN4, 174 more genes
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 MIR3074, PLPPR1, 242 more genes
    nsv4684056copy number variation1nstd102humanPathogenic GRCh37 chr9: 98,209,194-98,279,102 , GRCh38.p12 chr9: 95,446,912-95,516,820 LOC100507346, PTCH1
    nsv4682878copy number variation1nstd102humanUncertain significance GRCh37 chr9: 98,209,194-98,270,643 , GRCh38.p12 chr9: 95,446,912-95,508,361 PTCH1, LOC100507346
    nsv4681323copy number variation1nstd102humanPathogenic GRCh37 chr9: 98,209,194-98,279,100 , GRCh38.p12 chr9: 95,446,912-95,516,818 LOC100507346, PTCH1
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 LOC105376167, RNU6-1160P, 112 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
    nsv4456543copy number variation1nstd102humanPathogenic GRCh37 chr9: 98,156,960-99,345,624 , GRCh38.p12 chr9: 95,394,678-96,583,342 LOC105376157, LOC112268049, 27 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
    nsv4450326copy number variation1nstd102humanPathogenic GRCh38 chr9: 95,101,697-95,508,371 , GRCh37 chr9: 97,863,979-98,270,653 RNA5SP288, FANCC, 9 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
    nsv3963517copy number variation1nstd168human GRCh38 chr9: 95,455,744-95,485,309 , GRCh37.p13 chr9: 98,218,026-98,247,591 PTCH1, LOC100507346
    nsv3924164copy number variation1nstd102humanPathogenic GRCh38 chr9: 94,184,266-106,730,550 , GRCh37 chr9: 96,946,548-109,492,831 , NCBI36 chr9: 95,986,369-108,532,652 FYTTD1P1, MIR23B, 233 more genes
    nsv3922790copy number variation1nstd102humanPathogenic GRCh38 chr9: 94,713,892-98,121,186 , GRCh37 chr9: 97,476,174-100,883,468 , NCBI36 chr9: 96,515,995-99,923,289 HSD17B3-AS1, LOC105376159, 91 more genes
    nsv3922685copy number variation1nstd102humanPathogenic GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076 ECM2, RPL21P86, 480 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
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