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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045466inversion1nstd229human GRCh38 chr2: 106,066,400-106,069,515 , GRCh37.p13 chr2: 106,682,856-106,685,971 ECRG4
    nsv6696802copy number variation1nstd229human GRCh38 chr2: 106,078,622-106,079,438 , GRCh37.p13 chr2: 106,695,078-106,695,894 ECRG4
    nsv6695055copy number variation1nstd229human GRCh38 chr2: 106,059,825-106,065,229 , GRCh37.p13 chr2: 106,676,281-106,681,685 ECRG4
    nsv6692601copy number variation1nstd229human GRCh38 chr2: 106,073,213-106,087,907 , GRCh37.p13 chr2: 106,689,669-106,704,363 ECRG4
    nsv6692526copy number variation1nstd229human GRCh38 chr2: 105,790,869-106,321,112 , GRCh37.p13 chr2: 106,407,326-106,937,568 UXS1, RPL22P10, 7 more genes
    nsv6690636copy number variation1nstd229human GRCh38 chr2: 106,067,301-106,069,300 , GRCh37.p13 chr2: 106,683,757-106,685,756 ECRG4
    nsv6686545copy number variation1nstd229human GRCh38 chr2: 103,585,907-110,943,040 , GRCh37.p13 chr2: 104,202,365-111,700,617 PPP1R2P5, CAPZBP1, 142 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6553207inversion1nstd223human GRCh38 chr2: 106,067,074-106,067,772 , GRCh37.p13 chr2: 106,683,530-106,684,228 ECRG4
    nsv6548231inversion1nstd223human GRCh38 chr2: 106,062,622-106,066,658 , GRCh37.p13 chr2: 106,679,078-106,683,114 ECRG4
    nsv6354628copy number variation1nstd223human GRCh38 chr2: 106,078,622-106,079,438 , GRCh37.p13 chr2: 106,695,078-106,695,894 ECRG4
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6042811insertion1nstd212human GRCh38 chr2: 106,069,148-106,069,148 , GRCh37.p13 chr2: 106,685,604-106,685,604 ECRG4
    nsv5985290copy number variation1nstd212human GRCh38 chr2: 106,078,621-106,079,438 , GRCh37.p13 chr2: 106,695,077-106,695,894 ECRG4
    nsv5966119insertion1nstd209human GRCh38 chr2: 106,071,322-106,071,322 , GRCh37.p13 chr2: 106,687,778-106,687,778 ECRG4
    nsv5885050copy number variation1nstd209human GRCh38 chr2: 106,069,152-106,069,216 , GRCh37.p13 chr2: 106,685,608-106,685,672 ECRG4
    nsv5880276copy number variation1nstd209human GRCh38 chr2: 106,078,621-106,079,437 , GRCh37.p13 chr2: 106,695,077-106,695,893 ECRG4
    nsv5605391insertion1nstd207human GRCh38 chr2: 106,069,143-106,069,143 , GRCh37.p13 chr2: 106,685,599-106,685,599 ECRG4
    nsv5577929copy number variation1nstd207human GRCh38 chr2: 106,078,621-106,079,437 , GRCh37.p13 chr2: 106,695,077-106,695,893 ECRG4
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