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Items: 1 to 20 of 332

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056326inversion1nstd229human GRCh38 chr2: 134,976,570-134,982,386 , GRCh37.p13 chr2: 135,734,140-135,739,956 MAP3K19
    nsv6694720copy number variation1nstd229human GRCh38 chr2: 134,975,114-134,983,673 , GRCh37.p13 chr2: 135,732,684-135,741,243 MAP3K19
    nsv6694281copy number variation1nstd229human GRCh38 chr2: 134,910,646-134,975,494 , GRCh37.p13 chr2: 135,668,216-135,733,064 CCNT2, MAP3K19, 1 more genes
    nsv6688435copy number variation1nstd229human GRCh38 chr2: 134,973,322-134,977,430 , GRCh37.p13 chr2: 135,730,892-135,735,000 MAP3K19
    nsv6686111copy number variation1nstd229human GRCh38 chr2: 134,999,338-135,007,361 , GRCh37.p13 chr2: 135,756,908-135,764,931 MAP3K19
    nsv6685837copy number variation1nstd229human GRCh38 chr2: 134,924,524-134,962,465 , GRCh37.p13 chr2: 135,682,094-135,720,035 CCNT2, MAP3K19
    nsv6685676copy number variation1nstd229human GRCh38 chr2: 134,964,550-134,964,628 , GRCh37.p13 chr2: 135,722,120-135,722,198 MAP3K19
    nsv6685524copy number variation1nstd229human GRCh38 chr2: 134,986,908-134,992,266 , GRCh37.p13 chr2: 135,744,478-135,749,836 MAP3K19
    nsv6684581copy number variation1nstd229human GRCh38 chr2: 134,979,149-134,984,728 , GRCh37.p13 chr2: 135,736,719-135,742,298 MAP3K19
    nsv6682447copy number variation1nstd229human GRCh38 chr2: 135,003,401-135,181,200 , GRCh37.p13 chr2: 135,760,971-135,938,770 ZRANB3, SNORA40B, 2 more genes
    nsv6681893copy number variation1nstd229human GRCh38 chr2: 134,956,408-134,996,492 , GRCh37.p13 chr2: 135,713,978-135,754,062 CCNT2, MAP3K19
    nsv6679692copy number variation1nstd229human GRCh38 chr2: 128,625,642-138,426,614 , GRCh37.p13 chr2: 129,383,216-139,184,184 MTND4P27, LOC646674, 194 more genes
    nsv6627339copy number variation1nstd224human GRCh37 chr2: 135,699,619-136,374,311 , GRCh38.p12 chr2: 134,942,049-135,616,741 CCNT2, RAB3GAP1, 5 more genes
    nsv6552657inversion1nstd223human GRCh38 chr2: 135,034,937-135,036,058 , GRCh37.p13 chr2: 135,792,507-135,793,628 MAP3K19
    nsv6542175inversion1nstd223human GRCh38 chr2: 134,977,048-134,977,382 , GRCh37.p13 chr2: 135,734,618-135,734,952 MAP3K19
    nsv6541527inversion1nstd223human GRCh38 chr2: 135,018,894-135,020,013 , GRCh37.p13 chr2: 135,776,464-135,777,583 MAP3K19
    nsv6353244copy number variation1nstd223human GRCh38 chr2: 135,040,671-135,081,647 , GRCh37.p13 chr2: 135,798,241-135,839,217 MAP3K19, RAB3GAP1
    nsv6351740copy number variation1nstd223human GRCh38 chr2: 134,986,905-134,992,262 , GRCh37.p13 chr2: 135,744,475-135,749,832 MAP3K19
    nsv6349150copy number variation1nstd223human GRCh38 chr2: 134,994,364-134,994,715 , GRCh37.p13 chr2: 135,751,934-135,752,285 MAP3K19
    nsv6348249copy number variation1nstd223human GRCh38 chr2: 134,974,701-134,976,500 , GRCh37.p13 chr2: 135,732,271-135,734,070 MAP3K19
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