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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096244copy number variation1nstd102humanUncertain significance GRCh37 chr2: 227,659,726-228,567,034 , GRCh38.p12 chr2: 226,795,010-227,702,318 SLC19A3, IRS1, 12 more genes
    nsv7049962inversion1nstd229human GRCh38 chr2: 227,539,172-230,370,061 , GRCh37.p13 chr2: 228,403,888-231,234,776 SPHKAP, TRIP12, 37 more genes
    nsv7047209inversion1nstd229human GRCh38 chr2: 222,803,564-227,992,948 , GRCh37.p13 chr2: 223,668,283-228,857,664 MFF, LOC100289117, 55 more genes
    nsv7045781inversion1nstd229human GRCh38 chr2: 226,619,501-227,899,799 , GRCh37.p13 chr2: 227,484,217-228,764,515 SLC19A3, IRS1, 19 more genes
    nsv7043640inversion1nstd229human GRCh38 chr2: 222,841,128-228,011,478 , GRCh37.p13 chr2: 223,705,846-228,876,194 MFF-DT, LOC105373905, 55 more genes
    nsv6687990copy number variation1nstd229human GRCh38 chr2: 227,600,128-227,629,124 , GRCh37.p13 chr2: 228,464,844-228,493,840 C2orf83, LOC729968
    nsv6685948copy number variation1nstd229human GRCh38 chr2: 227,612,827-227,675,883 , GRCh37.p13 chr2: 228,477,543-228,540,599 LOC729968, C2orf83, 1 more genes
    nsv6685783copy number variation1nstd229human GRCh38 chr2: 227,614,657-227,614,742 , GRCh37.p13 chr2: 228,479,373-228,479,458 C2orf83
    nsv6685280copy number variation1nstd229human GRCh38 chr2: 227,608,990-227,617,693 , GRCh37.p13 chr2: 228,473,706-228,482,409 LOC729968, C2orf83
    nsv6680369copy number variation1nstd229human GRCh38 chr2: 227,606,882-227,647,817 , GRCh37.p13 chr2: 228,471,598-228,512,533 LOC100420667, C2orf83, 1 more genes
    nsv6680028copy number variation1nstd229human GRCh38 chr2: 227,608,869-227,617,617 , GRCh37.p13 chr2: 228,473,585-228,482,333 LOC729968, C2orf83
    nsv6678700copy number variation1nstd229human GRCh38 chr2: 226,880,942-228,292,097 , GRCh37.p13 chr2: 227,745,658-229,156,813 LOC107985993, LOC100533842, 21 more genes
    nsv6627634copy number variation1nstd224human GRCh37 chr2: 228,474,106-228,622,128 , GRCh38.p12 chr2: 227,609,390-227,757,412 SLC19A3, LOC729968, 2 more genes
    nsv6546353inversion1nstd223human GRCh38 chr2: 227,539,362-230,369,917 , GRCh37.p13 chr2: 228,404,078-231,234,632 FBXO36, LOC729968, 37 more genes
    nsv6541613inversion1nstd223human GRCh38 chr2: 227,618,688-227,618,828 , GRCh37.p13 chr2: 228,483,404-228,483,544 LOC729968, C2orf83
    nsv6541400inversion1nstd223human GRCh38 chr2: 227,539,172-230,370,025 , GRCh37.p13 chr2: 228,403,888-231,234,740 SNRPGP8, DNER, 37 more genes
    nsv6341496copy number variation1nstd223human GRCh38 chr2: 227,580,601-227,629,500 , GRCh37.p13 chr2: 228,445,317-228,494,216 LOC729968, C2orf83
    nsv6341478copy number variation1nstd223human GRCh38 chr2: 227,582,101-227,627,100 , GRCh37.p13 chr2: 228,446,817-228,491,816 LOC729968, C2orf83
    nsv6339848copy number variation1nstd223human GRCh38 chr2: 227,630,968-227,791,300 , GRCh37.p13 chr2: 228,495,684-228,656,016 LOC100420667, SNRPGP8, 3 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
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