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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143222copy number variation1nstd232human GRCh37.p13 chr1: 55,334,337-55,334,388 , GRCh38.p12 chr1: 54,868,664-54,868,715 DHCR24
    nsv7099206copy number variation1nstd231human GRCh38.p12 chr1: 54,693,460-58,571,894 , GRCh37 chr1: 55,159,133-59,037,566 C8A, C8B, 49 more genes
    nsv7095996copy number variation1nstd102humanUncertain significance GRCh37 chr1: 55,223,407-55,352,792 , GRCh38.p12 chr1: 54,757,734-54,887,119 CIMAP2, DHCR24, 3 more genes
    nsv7053230inversion1nstd229human GRCh38 chr1: 54,133,615-56,561,151 , GRCh37.p13 chr1: 54,599,288-57,026,824 GOT2P1, CIMAP2, 41 more genes
    nsv6651989copy number variation1nstd229human GRCh38 chr1: 54,876,465-54,877,079 , GRCh37.p13 chr1: 55,342,138-55,342,752 DHCR24
    nsv6651988copy number variation1nstd229human GRCh38 chr1: 54,859,801-54,862,500 , GRCh37.p13 chr1: 55,325,474-55,328,173 DHCR24
    nsv6651987copy number variation1nstd229human GRCh38 chr1: 54,858,161-54,863,960 , GRCh37.p13 chr1: 55,323,834-55,329,633 DHCR24
    nsv6651977copy number variation1nstd229human GRCh38 chr1: 54,882,791-54,896,762 , GRCh37.p13 chr1: 55,348,464-55,362,435 DHCR24-DT, DHCR24
    nsv6651976copy number variation1nstd229human GRCh38 chr1: 54,868,664-54,868,716 , GRCh37.p13 chr1: 55,334,337-55,334,389 DHCR24
    nsv6651975copy number variation1nstd229human GRCh38 chr1: 54,857,387-54,861,156 , GRCh37.p13 chr1: 55,323,060-55,326,829 DHCR24
    nsv6651974copy number variation1nstd229human GRCh38 chr1: 54,855,901-54,859,600 , GRCh37.p13 chr1: 55,321,574-55,325,273 DHCR24
    nsv6651970copy number variation1nstd229human GRCh38 chr1: 54,774,260-54,865,477 , GRCh37.p13 chr1: 55,239,933-55,331,150 TTC22, CIMAP2, 1 more genes
    nsv6651948copy number variation1nstd229human GRCh38 chr1: 54,489,332-54,940,292 , GRCh37.p13 chr1: 54,955,005-55,405,965 FAM151A, LINC02784, 12 more genes
    nsv6651887copy number variation1nstd229human GRCh38 chr1: 54,876,568-54,877,713 , GRCh37.p13 chr1: 55,342,241-55,343,386 DHCR24
    nsv6651884copy number variation1nstd229human GRCh38 chr1: 54,798,403-55,085,262 , GRCh37.p13 chr1: 55,264,076-55,550,935 PCSK9, TTC22, 8 more genes
    nsv6651229copy number variation1nstd229human GRCh38 chr1: 54,876,401-54,882,900 , GRCh37.p13 chr1: 55,342,074-55,348,573 DHCR24
    nsv6651228copy number variation1nstd229human GRCh38 chr1: 54,851,909-54,855,920 , GRCh37.p13 chr1: 55,317,582-55,321,593 DHCR24
    nsv6636008copy number variation1nstd102humanUncertain significance GRCh37 chr1: 55,334,341-55,334,393 , GRCh38 chr1: 54,868,668-54,868,720 DHCR24
    nsv6626459copy number variation1nstd224human GRCh37 chr1: 54,883,003-55,349,442 , GRCh38.p12 chr1: 54,417,330-54,883,769 DHCR24, FAM151A, 11 more genes
    nsv6626262copy number variation1nstd224human GRCh37 chr1: 54,887,297-55,324,869 , GRCh38.p12 chr1: 54,421,624-54,859,196 TALDO1P1, TTC4, 11 more genes
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