U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 91

    loading data ...

    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
    nsv5295678copy number variation1nstd204human GRCh38.p13 chr19: 12,445,401-12,989,100 , GRCh37.p13 chr19: 12,556,215-13,099,914 GCDH, RPL10P16, 46 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
    nsv5014544copy number variation1nstd200human GRCh38 chr19: 12,703,791-12,705,282 , GRCh37.p13 chr19: 12,814,605-12,816,096 TNPO2, SNORD135, 1 more genes
    nsv4864940copy number variation1nstd200human GRCh37 chr19: 12,814,605-12,816,096 , GRCh38.p12 chr19: 12,703,791-12,705,282 TNPO2, SNORD135, 1 more genes
    nsv4630529copy number variation2nstd183human GRCh37 chr19: 12,735,946-13,097,039 , GRCh38.p12 chr19: 12,625,132-12,986,225 MAST1, SNORD41, 35 more genes
    nsv4629336copy number variation1nstd183human GRCh37 chr19: 12,295,610-12,947,938 , GRCh38.p12 chr19: 12,184,795-12,837,124 , DHPS, 44 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
    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
    nsv3922999copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452 ZNF433, MIR6794, 155 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
    nsv3918107copy number variation1nstd102humanUncertain significance NCBI36 chr19: 12,329,719-12,739,860 , GRCh38 chr19: 12,357,905-12,768,046 , GRCh37 chr19: 12,468,719-12,878,860 MTATP6P27, BEST2, 29 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
    nsv3907864copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,574,343-14,726,197 , GRCh38.p12 chr19: 12,463,529-14,615,385 WDR83, DDX39A, 105 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center