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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093974copy number variation1nstd102humanUncertain significance GRCh37 chr12: 52,708,415-52,761,189 , GRCh38.p12 chr12: 52,314,631-52,367,405 KRT83, KRT89P, 1 more genes
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv7061604inversion1nstd229human GRCh38 chr12: 52,288,016-52,732,145 , GRCh37.p13 chr12: 52,681,800-53,125,929 KRT81, LOC400036, 22 more genes
    nsv6931004copy number variation1nstd229human GRCh38 chr12: 52,238,701-52,423,200 , GRCh37.p13 chr12: 52,632,485-52,816,984 KRT84, KRT89P, 11 more genes
    nsv6921500copy number variation1nstd229human GRCh38 chr12: 52,294,714-52,389,423 , GRCh37.p13 chr12: 52,688,498-52,783,207 KRT86, KRT83, 3 more genes
    nsv6621859copy number variation1nstd224human GRCh37 chr12: 52,700,040-52,779,113 , GRCh38.p12 chr12: 52,306,256-52,385,329 KRT85, KRT84, 3 more genes
    nsv6621820copy number variation1nstd224human GRCh37 chr12: 52,704,417-52,779,360 , GRCh38.p12 chr12: 52,310,633-52,385,576 KRT85, KRT89P, 2 more genes
    nsv6621819copy number variation1nstd224human GRCh37 chr12: 52,702,656-52,779,360 , GRCh38.p12 chr12: 52,308,872-52,385,576 KRT85, KRT84, 3 more genes
    nsv6621818copy number variation3nstd224human GRCh37 chr12: 52,702,656-52,778,829 , GRCh38.p12 chr12: 52,308,872-52,385,045 KRT85, KRT86, 3 more genes
    nsv6621817copy number variation1nstd224human GRCh37 chr12: 52,700,040-52,779,159 , GRCh38.p12 chr12: 52,306,256-52,385,375 KRT85, KRT89P, 3 more genes
    nsv6621816copy number variation2nstd224human GRCh37 chr12: 52,700,040-52,778,829 , GRCh38.p12 chr12: 52,306,256-52,385,045 KRT85, KRT89P, 3 more genes
    nsv6621815copy number variation2nstd224human GRCh37 chr12: 52,695,630-52,779,391 , GRCh38.p12 chr12: 52,301,846-52,385,607 KRT89P, KRT83, 3 more genes
    nsv6621814copy number variation1nstd224human GRCh37 chr12: 52,695,630-52,779,351 , GRCh38.p12 chr12: 52,301,846-52,385,567 KRT86, KRT89P, 3 more genes
    nsv6621813copy number variation1nstd224human GRCh37 chr12: 52,695,630-52,779,189 , GRCh38.p12 chr12: 52,301,846-52,385,405 KRT83, KRT86, 3 more genes
    nsv6621812copy number variation1nstd224human GRCh37 chr12: 52,695,630-52,779,003 , GRCh38.p12 chr12: 52,301,846-52,385,219 KRT83, KRT86, 3 more genes
    nsv6621811copy number variation1nstd224human GRCh37 chr12: 52,689,168-52,768,566 , GRCh38.p12 chr12: 52,295,384-52,374,782 KRT83, KRT86, 2 more genes
    nsv6621716copy number variation1nstd224human GRCh37 chr12: 52,710,663-52,777,513 , GRCh38.p12 chr12: 52,316,879-52,383,729 KRT85, KRT89P, 2 more genes
    nsv6621715copy number variation1nstd224human GRCh37 chr12: 52,704,417-52,779,008 , GRCh38.p12 chr12: 52,310,633-52,385,224 KRT89P, KRT83, 2 more genes
    nsv6621714copy number variation1nstd224human GRCh37 chr12: 52,702,656-52,779,351 , GRCh38.p12 chr12: 52,308,872-52,385,567 KRT86, KRT89P, 3 more genes
    nsv6621713copy number variation1nstd224human GRCh37 chr12: 52,702,656-52,779,006 , GRCh38.p12 chr12: 52,308,872-52,385,222 KRT83, KRT86, 3 more genes
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