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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5877491copy number variation1nstd209human GRCh38 chr19: 12,199,662-12,201,461 , GRCh37.p13 chr19: 12,310,477-12,312,276 LOC100289333
    nsv5167804mobile element insertion1nstd203human GRCh38 chr19: 12,193,051-12,193,067 , GRCh37.p13 chr19: 12,303,866-12,303,882 LOC100289333
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5011768copy number variation1nstd200human GRCh38 chr19: 12,201,683-12,210,600 , GRCh37.p13 chr19: 12,312,498-12,321,415 LOC100289333
    nsv5011767copy number variation1nstd200human GRCh38 chr19: 12,192,191-12,201,690 , GRCh37.p13 chr19: 12,303,006-12,312,505 LOC100289333
    nsv4860304copy number variation1nstd200human GRCh37 chr19: 12,312,498-12,321,415 , GRCh38.p12 chr19: 12,201,683-12,210,600 LOC100289333
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 SLC44A2, ZNF833P, 114 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
    nsv4544709insertion1nstd166human GRCh37.p13 chr19: 12,303,866-12,303,866 , GRCh38.p12 chr19: 12,193,051-12,193,051 LOC100289333
    nsv4451686copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 ODAD3, RNA5SP466, 114 more genes
    nsv4370574copy number variation1nstd173human GRCh37 chr19: 12,247,752-12,433,282 , GRCh38.p12 chr19: 12,136,937-12,322,468 , ZNF20, 10 more genes
    nsv4253549copy number variation1nstd166human GRCh37.p13 chr19: 12,315,900-12,322,000 , GRCh38.p12 chr19: 12,205,085-12,211,185 , LOC100289333
    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
    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
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