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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5381052copy number variation1nstd102humanUncertain significance GRCh37 chr19: 13,135,448-13,574,132 , GRCh38.p12 chr19: 13,024,634-13,463,318 IER2, CACNA1A, 7 more genes
    nsv5282549copy number variation1nstd204human GRCh38.p13 chr19: 12,584,101-13,543,500 , GRCh37.p13 chr19: 12,694,915-13,654,314 , NFIX, 50 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4860362copy number variation1nstd200human GRCh37 chr19: 13,259,477-13,260,157 , GRCh38.p12 chr19: 13,148,663-13,149,343 IER2, STX10
    nsv4647974copy number variation1nstd186human GRCh37 chr19: 13,259,500-13,266,500 , GRCh38.p12 chr19: 13,148,686-13,155,686 STX10, IER2
    nsv4625857copy number variation1nstd183human GRCh37 chr19: 13,260,571-13,267,998 , GRCh38.p12 chr19: 13,149,757-13,157,184 STX10, IER2, 1 more genes
    nsv4457524copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,354,642-13,424,014 , GRCh38.p12 chr19: 12,243,827-13,313,200 BEST2, TRMT1, 64 more genes
    nsv4255594copy number variation1nstd166human GRCh37.p13 chr19: 13,259,500-13,266,500 , GRCh38.p12 chr19: 13,148,686-13,155,686 IER2, STX10
    nsv3924844copy number variation1nstd102humanUncertain significance GRCh38 chr19: 12,978,943-13,236,134 , NCBI36 chr19: 12,950,757-13,207,948 , GRCh37 chr19: 13,089,757-13,346,948 LYL1, NFIX, 8 more genes
    nsv3924466copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833 JUNB, ZNF442, 135 more genes
    nsv3923415copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994 MAN2B1, SWSAP1, 182 more genes
    nsv3922964copy number variation1nstd102humanPathogenic GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674 SWSAP1, LOC105372284, 164 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3919036copy number variation1nstd102humanPathogenic GRCh37 chr19: 11,628,640-13,336,101 , NCBI36 chr19: 11,489,640-13,197,101 , GRCh38 chr19: 11,517,825-13,225,287 ZNF763, RTBDN, 105 more genes
    nsv3917896copy number variation1nstd102humanPathogenic NCBI36 chr19: 12,946,208-13,380,400 , GRCh38 chr19: 12,974,394-13,408,586 , GRCh37 chr19: 13,085,208-13,519,400 CACNA1A, DAND5, 9 more genes
    nsv3915970copy number variation1nstd102humanPathogenic NCBI36 chr19: 13,006,480-13,255,500 , GRCh37 chr19: 13,145,480-13,394,500 , GRCh38 chr19: 13,034,666-13,283,686 CACNA1A, LYL1, 7 more genes
    nsv3915094copy number variation1nstd102humanPathogenic GRCh38 chr19: 12,132,052-14,751,798 , NCBI36 chr19: 12,103,867-14,723,610 , GRCh37 chr19: 12,242,867-14,862,610 RN7SL619P, ZNF625-ZNF20, 123 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912480copy number variation1nstd102humanPathogenic GRCh38 chr19: 12,580,427-14,742,673 , GRCh37 chr19: 12,691,241-14,853,485 , NCBI36 chr19: 12,552,241-14,714,485 GET3, ADGRE3, 100 more genes
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