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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6644469copy number variation1nstd229human GRCh38 chr1: 169,443,352-169,449,006 , GRCh37.p13 chr1: 169,412,590-169,418,244 CCDC181
    nsv6644468copy number variation1nstd229human GRCh38 chr1: 169,371,980-169,409,874 , GRCh37.p13 chr1: 169,341,218-169,379,112 CCDC181, BLZF1
    nsv6644465copy number variation1nstd229human GRCh38 chr1: 169,282,980-169,437,910 , GRCh37.p13 chr1: 169,252,218-169,407,148 CCDC181, BLZF1, 1 more genes
    nsv6644401copy number variation1nstd229human GRCh38 chr1: 169,394,901-169,399,100 , GRCh37.p13 chr1: 169,364,139-169,368,338 CCDC181, BLZF1
    nsv6644298copy number variation1nstd229human GRCh38 chr1: 169,426,301-169,444,100 , GRCh37.p13 chr1: 169,395,539-169,413,338 CCDC181
    nsv6644256copy number variation1nstd229human GRCh38 chr1: 168,110,598-170,953,728 , GRCh37.p13 chr1: 168,079,836-170,922,869 SELL, RPL7AP21, 55 more genes
    nsv6644031copy number variation1nstd229human GRCh38 chr1: 169,405,205-169,407,958 , GRCh37.p13 chr1: 169,374,443-169,377,196 CCDC181
    nsv6637036copy number variation1nstd102humanUncertain significance GRCh37 chr1: 168,675,820-169,363,333 , GRCh38.p12 chr1: 168,706,582-169,394,095 LOC101928596, CCDC181, 10 more genes
    nsv6625915copy number variation1nstd224human GRCh37 chr1: 169,256,570-169,377,123 , GRCh38.p12 chr1: 169,287,332-169,407,885 BLZF1, NME7, 1 more genes
    nsv6546312inversion1nstd223human GRCh38 chr1: 169,446,443-169,447,124 , GRCh37.p13 chr1: 169,415,681-169,416,362 CCDC181
    nsv6545422inversion1nstd223human GRCh38 chr1: 169,446,404-169,447,313 , GRCh37.p13 chr1: 169,415,642-169,416,551 CCDC181
    nsv6536449inversion1nstd223human GRCh38 chr1: 169,227,760-169,402,827 , GRCh37.p13 chr1: 169,196,998-169,372,065 BLZF1, NME7, 1 more genes
    nsv6332420copy number variation1nstd223human GRCh38 chr1: 169,401,200-169,402,674 , GRCh37.p13 chr1: 169,370,438-169,371,912 CCDC181
    nsv6332026copy number variation1nstd223human GRCh38 chr1: 169,421,420-169,421,922 , GRCh37.p13 chr1: 169,390,658-169,391,160 CCDC181
    nsv6328533copy number variation1nstd223human GRCh38 chr1: 169,439,960-169,440,338 , GRCh37.p13 chr1: 169,409,198-169,409,576 CCDC181
    nsv6328327copy number variation1nstd223human GRCh38 chr1: 169,432,601-169,436,100 , GRCh37.p13 chr1: 169,401,839-169,405,338 CCDC181
    nsv6327054copy number variation1nstd223human GRCh38 chr1: 169,443,352-169,449,006 , GRCh37.p13 chr1: 169,412,590-169,418,244 CCDC181
    nsv6326642copy number variation1nstd223human GRCh38 chr1: 169,404,744-169,411,880 , GRCh37.p13 chr1: 169,373,982-169,381,118 CCDC181
    nsv6326484copy number variation1nstd223human GRCh38 chr1: 169,420,101-169,421,300 , GRCh37.p13 chr1: 169,389,339-169,390,538 CCDC181
    nsv6325509copy number variation1nstd223human GRCh38 chr1: 169,424,001-169,424,800 , GRCh37.p13 chr1: 169,393,239-169,394,038 CCDC181
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