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Items: 13

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    Number of Variants: 13

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093978copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,720,586-65,722,403 , GRCh38.p12 chr12: 65,326,806-65,328,623 MSRB3
    nsv3901540copy number variation1nstd102humanUncertain significance GRCh37 chr12: 65,656,429-65,678,117 , GRCh38.p12 chr12: 65,262,649-65,284,337 MSRB3
    nsv3897901copy number variation1nstd102humanBenign GRCh37 chr12: 65,898,179-66,018,473 , GRCh38.p12 chr12: 65,504,399-65,624,693 LOC105369806, LOC105369808, 3 more genes
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 MSRB3, LINC02421, 144 more genes
    nsv7093395copy number variation1nstd102humanPathogenic GRCh37 chr12: 64,609,458-70,352,103 , GRCh38.p12 chr12: 64,215,678-69,958,323 MSRB3, TODL, 116 more genes
    nsv3916302copy number variation1nstd102humanPathogenic NCBI36 chr12: 59,587,199-65,248,124 , GRCh37 chr12: 61,300,932-66,961,857 , GRCh38 chr12: 60,907,151-66,568,077 MSRB3, LOC105369809, 93 more genes
    nsv3911433copy number variation1nstd102humanPathogenic NCBI36 chr12: 64,125,223-69,706,384 , GRCh38 chr12: 65,445,176-71,026,337 , GRCh37 chr12: 65,838,956-71,420,117 MSRB3, SLC35E3, 100 more genes
    nsv7094153copy number variation1nstd102humanPathogenic GRCh37 chr12: 64,849,651-65,857,102 , GRCh38.p12 chr12: 64,455,871-65,463,322 MSRB3, GNS, 18 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 MSRB3, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 MSRB3, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 MSRB3, RNU4ATAC16P, 2452 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 MSRB3, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 MSRB3, OR5BT1P, 2441 more genes
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