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Items: 1 to 20 of 248

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966132insertion1nstd209human GRCh38 chr3: 185,194,800-185,194,800 , GRCh37.p13 chr3: 184,912,588-184,912,588 EHHADH
    nsv5965311insertion1nstd209human GRCh38 chr3: 185,228,257-185,228,257 , GRCh37.p13 chr3: 184,946,045-184,946,045 EHHADH
    nsv5957760insertion1nstd209human GRCh38 chr3: 185,236,389-185,236,389 , GRCh37.p13 chr3: 184,954,177-184,954,177 EHHADH
    nsv5890460copy number variation1nstd209human GRCh38 chr3: 185,183,837-185,198,019 , GRCh37.p13 chr3: 184,901,625-184,915,807 EHHADH-AS1, EHHADH
    nsv5834826copy number variation1nstd209human GRCh38 chr3: 185,183,802-185,197,590 , GRCh37.p13 chr3: 184,901,590-184,915,378 EHHADH, EHHADH-AS1
    nsv5730096mobile element insertion1nstd211human GRCh38 chr3: 185,253,594-185,253,594 , GRCh37.p13 chr3: 184,971,382-184,971,382 EHHADH, MIR5588
    nsv5677200mobile element insertion1nstd211human GRCh38 chr3: 185,197,342-185,197,342 , GRCh37.p13 chr3: 184,915,130-184,915,130 EHHADH
    nsv5615201insertion1nstd207human GRCh38 chr3: 185,228,632-185,228,632 , GRCh37.p13 chr3: 184,946,420-184,946,420 EHHADH
    nsv5614962insertion1nstd207human GRCh38 chr3: 185,236,389-185,236,389 , GRCh37.p13 chr3: 184,954,177-184,954,177 EHHADH
    nsv5581577copy number variation1nstd207human GRCh38 chr3: 185,230,658-185,231,224 , GRCh37.p13 chr3: 184,948,446-184,949,012 EHHADH
    nsv5574023copy number variation1nstd207human GRCh38 chr3: 185,234,489-185,234,589 , GRCh37.p13 chr3: 184,952,277-184,952,377 EHHADH
    nsv5571392copy number variation1nstd207human GRCh38 chr3: 185,230,621-185,230,863 , GRCh37.p13 chr3: 184,948,409-184,948,651 EHHADH
    nsv5565465copy number variation1nstd207human GRCh38 chr3: 185,230,658-185,230,738 , GRCh37.p13 chr3: 184,948,446-184,948,526 EHHADH
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5442076copy number variation1nstd206human GRCh38 chr3: 185,183,797-185,198,071 , GRCh37.p13 chr3: 184,901,585-184,915,859 EHHADH, EHHADH-AS1
    nsv5393976mobile element insertion1nstd206human GRCh38 chr3: 185,197,342-185,197,393 , GRCh37.p13 chr3: 184,915,130-184,915,181 EHHADH
    nsv5093913mobile element insertion1nstd203human GRCh38 chr3: 185,239,941-185,239,953 , GRCh37.p13 chr3: 184,957,729-184,957,741 EHHADH
    nsv5092077mobile element insertion1nstd203human GRCh38 chr3: 185,249,287-185,249,301 , GRCh37.p13 chr3: 184,967,075-184,967,089 EHHADH
    nsv5080720mobile element insertion1nstd203human GRCh38 chr3: 185,228,211-185,228,233 , GRCh37.p13 chr3: 184,945,999-184,946,021 EHHADH
    nsv4921235copy number variation1nstd200human GRCh38 chr3: 185,228,880-185,262,404 , GRCh37.p13 chr3: 184,946,668-184,980,192 EIF2S2P2, EHHADH, 1 more genes
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