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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv6714805copy number variation1nstd229human GRCh38 chr3: 100,633,956-100,639,066 , GRCh37.p13 chr3: 100,352,800-100,357,910 ADGRG7
    nsv6714237copy number variation1nstd229human GRCh38 chr3: 100,694,509-100,701,681 , GRCh37.p13 chr3: 100,413,353-100,420,525 ADGRG7
    nsv6706416copy number variation1nstd229human GRCh38 chr3: 100,678,079-100,690,029 , GRCh37.p13 chr3: 100,396,923-100,408,873 ADGRG7
    nsv6705166copy number variation1nstd229human GRCh38 chr3: 100,616,027-100,727,313 , GRCh37.p13 chr3: 100,334,871-100,446,157 TFG, GMFBP1, 1 more genes
    nsv6704284copy number variation1nstd229human GRCh38 chr3: 100,604,875-100,608,439 , GRCh37.p13 chr3: 100,323,719-100,327,283 ADGRG7
    nsv6635963copy number variation1nstd227human GRCh37 chr3: 100,351,696-100,467,018 , GRCh38.p12 chr3: 100,632,852-100,748,174 TFG, ABI3BP, 2 more genes
    nsv6635917copy number variation2nstd227human GRCh37 chr3: 100,324,522-100,437,892 , GRCh38.p12 chr3: 100,605,678-100,719,048 TFG, ADGRG7, 1 more genes
    nsv6635599copy number variation2nstd227human GRCh37 chr3: 100,351,696-100,507,827 , GRCh38.p12 chr3: 100,632,852-100,788,983 TFG, ABI3BP, 2 more genes
    nsv6634817copy number variation1nstd227human GRCh37 chr3: 100,351,696-100,468,500 , GRCh38.p12 chr3: 100,632,852-100,749,656 TFG, ABI3BP, 2 more genes
    nsv6634801copy number variation16nstd227human GRCh37 chr3: 100,351,696-100,437,892 , GRCh38.p12 chr3: 100,632,852-100,719,048 TFG, ADGRG7, 1 more genes
    nsv6634731copy number variation1nstd227human GRCh37 chr3: 100,334,256-100,437,892 , GRCh38.p12 chr3: 100,615,412-100,719,048 TFG, ADGRG7, 1 more genes
    nsv6628613copy number variation2nstd224human GRCh37 chr3: 100,354,524-100,427,937 , GRCh38.p12 chr3: 100,635,680-100,709,093 GMFBP1, TFG, 1 more genes
    nsv6628612copy number variation2nstd224human GRCh37 chr3: 100,352,109-100,427,937 , GRCh38.p12 chr3: 100,633,265-100,709,093 TFG, GMFBP1, 1 more genes
    nsv6628434copy number variation1nstd224human GRCh37 chr3: 100,352,223-100,427,937 , GRCh38.p12 chr3: 100,633,379-100,709,093 GMFBP1, TFG, 1 more genes
    nsv6628433copy number variation4nstd224human GRCh37 chr3: 100,351,696-100,413,760 , GRCh38.p12 chr3: 100,632,852-100,694,916 ADGRG7, GMFBP1
    nsv6628246copy number variation29nstd224human GRCh37 chr3: 100,355,338-100,441,859 , GRCh38.p12 chr3: 100,636,494-100,723,015 TFG, ADGRG7, 1 more genes
    nsv6628245copy number variation1nstd224human GRCh37 chr3: 100,354,623-100,427,937 , GRCh38.p12 chr3: 100,635,779-100,709,093 TFG, ADGRG7, 1 more genes
    nsv6628187copy number variation4nstd224human GRCh37 chr3: 100,352,151-100,427,937 , GRCh38.p12 chr3: 100,633,307-100,709,093 TFG, ADGRG7, 1 more genes
    nsv6628186copy number variation71nstd224human GRCh37 chr3: 100,351,696-100,427,937 , GRCh38.p12 chr3: 100,632,852-100,709,093 TFG, ADGRG7, 1 more genes
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