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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880878copy number variation1nstd209human GRCh38 chr2: 20,908,225-21,523,658 , GRCh37.p13 chr2: 21,107,985-21,746,530 APOB, TDRD15, 4 more genes
    nsv5691497mobile element insertion2nstd211human GRCh38 chr2: 21,016,989-21,016,989 , GRCh37.p13 chr2: 21,239,861-21,239,861 APOB
    nsv5690286mobile element insertion2nstd211human GRCh38 chr2: 21,040,664-21,040,664 , GRCh37.p13 chr2: 21,263,536-21,263,536 APOB
    nsv5617504insertion1nstd207human GRCh38 chr2: 21,001,174-21,001,174 , GRCh37.p13 chr2: 21,224,046-21,224,046 APOB
    nsv5607617insertion1nstd207human GRCh38 chr2: 21,001,219-21,001,219 , GRCh37.p13 chr2: 21,224,091-21,224,091 APOB
    nsv5576265copy number variation1nstd207human GRCh38 chr2: 21,000,846-21,000,995 , GRCh37.p13 chr2: 21,223,718-21,223,867 APOB
    nsv5576197copy number variation1nstd207human GRCh38 chr2: 21,000,951-21,001,010 , GRCh37.p13 chr2: 21,223,823-21,223,882 APOB
    nsv5566618copy number variation1nstd207human GRCh38 chr2: 21,001,069-21,001,203 , GRCh37.p13 chr2: 21,223,941-21,224,075 APOB
    nsv5400818mobile element insertion1nstd206human GRCh38 chr2: 21,040,664-21,040,715 , GRCh37.p13 chr2: 21,263,536-21,263,587 APOB
    nsv4900545copy number variation1nstd200human GRCh38 chr2: 21,000,518-21,022,373 , GRCh37.p13 chr2: 21,223,390-21,245,245 APOB
    nsv4755629insertion1nstd199human GRCh37 chr2: 21,223,878-21,223,878 , GRCh38.p12 chr2: 21,001,006-21,001,006 APOB
    nsv4466189mobile element insertion1nstd166human GRCh37.p13 chr2: 21,263,520-21,263,520 , GRCh38.p12 chr2: 21,040,648-21,040,648 APOB
    nsv4451022copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621 RAD51AP2, LOC101928149, 82 more genes
    nsv4335876sequence alteration1nstd166human GRCh37.p13 chr2: 20,021,666-53,788,063 , GRCh38.p12 chr2: 19,821,905-53,560,926 , ADCY3, 531 more genes
    nsv4068986copy number variation1nstd166human GRCh37.p13 chr2: 21,249,351-21,250,841 , GRCh38.p12 chr2: 21,026,479-21,027,969 APOB
    nsv4053324copy number variation1nstd166human GRCh37.p13 chr2: 21,252,087-21,253,063 , GRCh38.p12 chr2: 21,029,215-21,030,191 APOB
    nsv3947239insertion1nstd167human GRCh37 chr2: 21,224,015-21,224,015 , GRCh38.p12 chr2: 21,001,143-21,001,143 APOB
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SLC35F6, LOC105374458, 801 more genes
    nsv3908459copy number variation1nstd102humanPathogenic NCBI36 chr2: 1,647,394-23,740,517 , GRCh38 chr2: 1,664,615-23,664,142 , GRCh37 chr2: 1,668,387-23,887,012 EIF1P7, LOC105373398, 277 more genes
    nsv3908288copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875 ALLC, LOC105373429, 674 more genes
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