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Items: 19

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    Number of Variants: 19

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3892873copy number variation1nstd102humanLikely benign GRCh37 chr19: 11,039,101-11,040,126 , GRCh38.p12 chr19: 10,928,425-10,929,450 YIPF2, TIMM29
    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 YIPF2, SWSAP1, 164 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 YIPF2, ZNF433, 155 more genes
    nsv3912242copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677 YIPF2, PPAN, 68 more genes
    nsv3900924copy number variation1nstd102humanPathogenic GRCh37 chr19: 10,286,133-11,040,457 , GRCh38.p12 chr19: 10,175,457-10,929,781 YIPF2, MIR4322, 38 more genes
    nsv4729806copy number variation1nstd102humanPathogenic GRCh37 chr19: 10,957,601-11,672,041 , GRCh38.p12 chr19: 10,846,925-11,561,226 YIPF2, DOCK6-AS1, 32 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 YIPF2, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 YIPF2, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 YIPF2, LENG8, 2408 more genes
    nsv3898900copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614 YIPF2, FBXL12, 253 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 YIPF2, MAN2B1, 182 more genes
    nsv3922509copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 10,302,331-10,892,228 , GRCh37 chr19: 10,441,331-11,031,228 , GRCh38 chr19: 10,330,655-10,920,552 YIPF2, CDKN2D, 26 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 YIPF2, ACP5, 236 more genes
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 YIPF2, SLC44A2, 114 more genes
    nsv4451686copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 YIPF2, ODAD3, 114 more genes
    nsv7095458copy number variation4nstd102humanUncertain significance GRCh37 chr19: 10,828,919-13,482,613 , GRCh38.p12 chr19: 10,718,243-13,371,799 YIPF2, WDR83OS, 140 more genes
    nsv6291543copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752 YIPF2, KRI1, 88 more genes
    nsv4676283copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,632,623-11,135,294 , GRCh38.p12 chr19: 10,521,947-11,024,618 YIPF2, ATG4D, 21 more genes
    nsv5381193copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,912,954-11,200,309 , GRCh38.p12 chr19: 10,802,278-11,089,633 YIPF2, SMARCA4, 10 more genes
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