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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6722565copy number variation1nstd229human GRCh38 chr3: 149,379,081-149,384,474 , GRCh37.p13 chr3: 149,096,868-149,102,261 TM4SF1-AS1
    nsv6363205copy number variation1nstd223human GRCh38 chr3: 149,364,882-149,367,286 , GRCh37.p13 chr3: 149,082,669-149,085,073 TM4SF1
    nsv5991819copy number variation1nstd212human GRCh38 chr3: 149,380,242-149,380,313 , GRCh37.p13 chr3: 149,098,029-149,098,100 TM4SF1-AS1
    nsv5894880copy number variation1nstd209human GRCh38 chr3: 149,380,188-149,380,351 , GRCh37.p13 chr3: 149,097,975-149,098,138 TM4SF1-AS1
    nsv3273070mobile element deletion1nstd152human GRCh38 chr3: 149,380,531-149,380,737 , GRCh37.p13 chr3: 149,098,318-149,098,524 TM4SF1-AS1
    nsv3362135copy number variation7nstd162human GRCh38 chr3: 149,380,246-149,380,314 , GRCh37.p13 chr3: 149,098,033-149,098,101 TM4SF1-AS1
    nsv2807786copy number variation1nstd137human GRCh38 chr3: 149,380,246-149,380,314 , GRCh37.p13 chr3: 149,098,033-149,098,101 TM4SF1-AS1
    esv3041816copy number variation1estd209human GRCh37 chr3: 149,102,584-149,102,585 , GRCh38.p12 chr3: 149,384,797-149,384,798 TM4SF1-AS1
    esv3041815copy number variation1estd209human GRCh37 chr3: 149,086,750-149,086,751 , GRCh38.p12 chr3: 149,368,963-149,368,964 TM4SF1
    esv3358372copy number variation8estd59human NCBI36 chr3: 150,579,577-150,582,125 , GRCh37.p13 chr3: 149,096,887-149,099,435 , GRCh38.p12 chr3: 149,379,100-149,381,648 TM4SF1-AS1
    esv2566424copy number variation1estd197human NCBI36 chr3: 150,586,197-150,586,197 , GRCh37.p13 chr3: 149,103,507-149,103,507 , GRCh38.p12 chr3: 149,385,720-149,385,720 TM4SF1-AS1
    esv2273386copy number variation1estd194human NCBI36 chr3: 150,585,274-150,585,275 , GRCh37.p13 chr3: 149,102,584-149,102,585 , GRCh38.p12 chr3: 149,384,797-149,384,798 TM4SF1-AS1
    esv2175448copy number variation1estd194human NCBI36 chr3: 150,569,441-150,569,442 , GRCh37.p13 chr3: 149,086,751-149,086,752 , GRCh38.p12 chr3: 149,368,964-149,368,965 TM4SF1
    esv2012727copy number variation1estd194human NCBI36 chr3: 150,586,197-150,586,198 , GRCh37.p13 chr3: 149,103,507-149,103,508 , GRCh38.p12 chr3: 149,385,720-149,385,721 TM4SF1-AS1
    esv1685355copy number variation1estd22human NCBI36 chr3: 150,585,285-150,585,286 , GRCh37.p13 chr3: 149,102,595-149,102,596 , GRCh38.p12 chr3: 149,384,808-149,384,809 TM4SF1-AS1
    esv1649088copy number variation1estd22human NCBI36 chr3: 150,569,450-150,569,451 , GRCh37.p13 chr3: 149,086,760-149,086,761 , GRCh38.p12 chr3: 149,368,973-149,368,974 TM4SF1
    nsv225465copy number variation1nstd6human NCBI35 chr3: 150,587,378-150,587,379 , GRCh37.p13 chr3: 149,104,680-149,104,681 , GRCh38.p12 chr3: 149,386,893-149,386,894 TM4SF1-AS1
    nsv6724432copy number variation1nstd229human GRCh38 chr3: 149,385,486-149,385,673 , GRCh37.p13 chr3: 149,103,273-149,103,460 TM4SF1-AS1
    nsv6728079copy number variation1nstd229human GRCh38 chr3: 149,373,720-149,373,784 , GRCh37.p13 chr3: 149,091,507-149,091,571 TM4SF1
    nsv5991603copy number variation1nstd212human GRCh38 chr3: 149,380,081-149,380,876 , GRCh37.p13 chr3: 149,097,868-149,098,663 TM4SF1-AS1
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