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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097208copy number variation1nstd102humanUncertain significance GRCh37 chr3: 53,736,648-53,845,433 , GRCh38.p12 chr3: 53,702,621-53,811,406 CHDH, CACNA1D
    nsv7097207copy number variation1nstd102humanUncertain significance GRCh37 chr3: 53,529,194-53,845,433 , GRCh38.p12 chr3: 53,495,167-53,811,406 CHDH, CACNA1D
    nsv7096962copy number variation1nstd102humanUncertain significance GRCh37 chr3: 53,820,829-53,845,433 , GRCh38.p12 chr3: 53,786,802-53,811,406 CACNA1D, CHDH
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv7054871inversion1nstd229human GRCh38 chr3: 53,658,161-53,683,109 , GRCh37.p13 chr3: 53,692,188-53,717,136 CACNA1D
    nsv7053982inversion1nstd229human GRCh38 chr3: 53,729,011-53,729,523 , GRCh37.p13 chr3: 53,763,038-53,763,550 CACNA1D
    nsv7051549inversion1nstd229human GRCh38 chr3: 53,729,214-53,729,436 , GRCh37.p13 chr3: 53,763,241-53,763,463 CACNA1D
    nsv7048768inversion1nstd229human GRCh38 chr3: 53,524,812-53,533,790 , GRCh37.p13 chr3: 53,558,839-53,567,817 CACNA1D
    nsv7044994inversion1nstd229human GRCh38 chr3: 53,780,997-53,781,076 , GRCh37.p13 chr3: 53,815,024-53,815,103 CACNA1D
    nsv7042717inversion1nstd229human GRCh38 chr3: 53,684,101-53,685,542 , GRCh37.p13 chr3: 53,718,128-53,719,569 CACNA1D
    nsv7040746inversion1nstd229human GRCh38 chr3: 53,527,985-53,533,652 , GRCh37.p13 chr3: 53,562,012-53,567,679 CACNA1D
    nsv7038956inversion1nstd229human GRCh38 chr3: 53,793,888-53,793,978 , GRCh37.p13 chr3: 53,827,915-53,828,005 CACNA1D
    nsv7038369inversion1nstd229human GRCh38 chr3: 53,553,582-53,560,958 , GRCh37.p13 chr3: 53,587,609-53,594,985 CACNA1D
    nsv6717465copy number variation1nstd229human GRCh38 chr3: 53,696,960-53,699,277 , GRCh37.p13 chr3: 53,730,987-53,733,304 CACNA1D
    nsv6716707copy number variation1nstd229human GRCh38 chr3: 53,767,647-53,833,678 , GRCh37.p13 chr3: 53,801,674-53,867,705 CACNA1D, CHDH
    nsv6716120copy number variation1nstd229human GRCh38 chr3: 53,687,201-53,694,100 , GRCh37.p13 chr3: 53,721,228-53,728,127 CACNA1D
    nsv6715685copy number variation1nstd229human GRCh38 chr3: 53,730,462-53,731,210 , GRCh37.p13 chr3: 53,764,489-53,765,237 CACNA1D
    nsv6715022copy number variation1nstd229human GRCh38 chr3: 53,747,463-53,768,783 , GRCh37.p13 chr3: 53,781,490-53,802,810 CACNA1D
    nsv6713202copy number variation1nstd229human GRCh38 chr3: 53,452,579-53,559,032 , GRCh37.p13 chr3: 53,486,606-53,593,059 CACNA1D, RPS25P4
    nsv6712502copy number variation1nstd229human GRCh38 chr3: 52,907,701-53,526,800 , GRCh37.p13 chr3: 52,941,717-53,560,827 SNORD38C, LOC107986087, 9 more genes
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