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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5693636mobile element insertion1nstd211human GRCh38 chr2: 9,613,828-9,613,828 , GRCh37.p13 chr2: 9,753,957-9,753,957 YWHAQ
    nsv5578486copy number variation1nstd207human GRCh38 chr2: 9,602,836-9,602,887 , GRCh37.p13 chr2: 9,742,965-9,743,016 YWHAQ
    nsv5452017copy number variation1nstd206human GRCh38 chr2: 9,630,566-9,630,625 , GRCh37.p13 chr2: 9,770,695-9,770,754 YWHAQ
    nsv5409949mobile element insertion1nstd206human GRCh38 chr2: 9,613,828-9,613,879 , GRCh37.p13 chr2: 9,753,957-9,754,008 YWHAQ
    nsv5071634mobile element insertion1nstd203human GRCh38 chr2: 9,613,812-9,613,828 , GRCh37.p13 chr2: 9,753,941-9,753,957 YWHAQ
    nsv5067899mobile element insertion1nstd203human GRCh38 chr2: 9,602,874-9,602,874 , GRCh37.p13 chr2: 9,743,003-9,743,003 YWHAQ
    nsv4892290copy number variation1nstd200human GRCh38 chr2: 9,618,502-9,623,173 , GRCh37.p13 chr2: 9,758,631-9,763,302 YWHAQ
    nsv4892289copy number variation1nstd200human GRCh38 chr2: 9,602,856-9,603,652 , GRCh37.p13 chr2: 9,742,985-9,743,781 YWHAQ
    nsv4892288copy number variation1nstd200human GRCh38 chr2: 9,602,471-9,615,904 , GRCh37.p13 chr2: 9,742,600-9,756,033 YWHAQ
    nsv4770141copy number variation1nstd200human GRCh37 chr2: 9,742,926-9,743,672 , GRCh38.p12 chr2: 9,602,797-9,603,543 YWHAQ
    nsv4468117mobile element insertion1nstd166human GRCh37.p13 chr2: 9,753,941-9,753,941 , GRCh38.p12 chr2: 9,613,812-9,613,812 YWHAQ
    nsv4069432copy number variation1nstd166human GRCh37.p13 chr2: 9,722,679-9,722,796 , GRCh38.p12 chr2: 9,582,550-9,582,667 YWHAQ
    nsv4068178copy number variation1nstd166human GRCh37.p13 chr2: 9,758,631-9,763,302 , GRCh38.p12 chr2: 9,618,502-9,623,173 YWHAQ
    nsv4058125copy number variation1nstd166human GRCh37.p13 chr2: 9,742,336-9,743,019 , GRCh38.p12 chr2: 9,602,207-9,602,890 YWHAQ
    nsv3969160insertion1nstd168human GRCh38 chr2: 9,560,950-9,586,004 , GRCh37.p13 chr2: 9,701,079-9,726,133 YWHAQ, LOC101929643
    nsv3908896copy number variation1nstd102humanPathogenic GRCh37 chr2: 6,671,304-16,243,921 , GRCh38 chr2: 6,531,172-16,103,799 , NCBI36 chr2: 6,588,755-16,161,372 RNU6-1288P, MIR7515HG, 138 more genes
    nsv3908628copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,342-14,924,526 , GRCh37 chr2: 30,342-15,007,075 , GRCh38 chr2: 30,342-14,866,951 RPS7, RPL30P3, 198 more genes
    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
    nsv3908405copy number variation1nstd102humanPathogenic GRCh38 chr2: 17,019-20,001,056 , NCBI36 chr2: 7,019-20,064,298 , GRCh37 chr2: 17,019-20,200,817 LOC100996549, LOC105373479, 252 more genes
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