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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5564430copy number variation1nstd102humanUncertain significance GRCh37 chr2: 29,119,585-29,450,548 , GRCh38.p12 chr2: 28,896,719-29,227,682 SNORD92, LOC105374386, 7 more genes
    nsv5564185copy number variation1nstd102humanUncertain significance GRCh37 chr2: 29,119,585-30,143,525 , GRCh38.p12 chr2: 28,896,719-29,920,659 WDR43, CLIP4, 10 more genes
    nsv4674305copy number variation1nstd102humanUncertain significance GRCh37 chr2: 28,387,514-29,616,031 , GRCh38.p12 chr2: 28,164,647-29,393,165 BABAM2, FOSL2, 27 more genes
    nsv4454993copy number variation1nstd102humanUncertain significance GRCh37 chr2: 28,980,521-29,300,911 , GRCh38.p12 chr2: 28,757,655-29,078,045 SNORD53B, PCARE, 7 more genes
    nsv4452277copy number variation1nstd102humanUncertain significance GRCh37 chr2: 29,030,646-29,289,738 , GRCh38.p12 chr2: 28,807,780-29,066,872 PCARE, SNORD53B, 6 more genes
    nsv4335876sequence alteration1nstd166human GRCh37.p13 chr2: 20,021,666-53,788,063 , GRCh38.p12 chr2: 19,821,905-53,560,926 , ADCY3, 531 more genes
    nsv4318621inversion1nstd166human GRCh37.p13 chr2: 21,612,232-41,909,281 , GRCh38.p12 chr2: 21,389,360-41,682,141 , CAD, 329 more genes
    nsv3919769copy number variation1nstd102humanPathogenic NCBI36 chr2: 22,776,056-33,845,581 , GRCh37.p13 chr2: 22,922,551-33,992,077 , GRCh38.p12 chr2: 22,699,679-33,767,010 RNA5SP88, EIF2B4, 213 more genes
    nsv3918250copy number variation1nstd102humanUncertain significance NCBI36 chr2: 28,976,219-29,155,149 , GRCh37.p13 chr2: 29,122,715-29,301,645 , GRCh38.p12 chr2: 28,899,849-29,078,779 SNORD92, TOGARAM2, 4 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SLC35F6, LOC105374458, 801 more genes
    nsv3908288copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875 ALLC, LOC105373429, 674 more genes
    nsv3908038copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509 LOC105373394, PGAM1P6, 507 more genes
    nsv3906963copy number variation1nstd102humanUncertain significance NCBI36 chr2: 28,633,816-29,514,013 , GRCh37 chr2: 28,780,312-29,660,509 , GRCh38 chr2: 28,557,445-29,437,643 PPP1CB, TRMT61B, 16 more genes
    nsv3906875copy number variation1nstd102humanUncertain significance GRCh37 chr2: 28,796,978-29,665,061 , GRCh38 chr2: 28,574,111-29,442,195 , NCBI36 chr2: 28,650,482-29,518,565 LOC105374386, TRMT61B, 16 more genes
    nsv3905458copy number variation1nstd102humanUncertain significance GRCh38 chr2: 28,561,270-29,446,956 , NCBI36 chr2: 28,637,641-29,523,326 , GRCh37 chr2: 28,784,137-29,669,822 PLB1, TOGARAM2, 16 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 LOC101927723, SANBR, 1246 more genes
    nsv3901052copy number variation1nstd102humanUncertain significance NCBI36 chr2: 28,765,595-29,030,516 , GRCh38 chr2: 28,689,225-28,954,146 , GRCh37 chr2: 28,912,091-29,177,012 PPP1CB, TRMT61B, 7 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNU6-674P, KANSL3, 3735 more genes
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