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Items: 1 to 20 of 1068

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137692copy number variation1nstd102humanLikely benign GRCh37 chr13: 111,145,433-111,145,496 , GRCh38 chr13: 110,493,086-110,493,149 COL4A2
    nsv6122013copy number variation1nstd186human GRCh37 chr13: 110,965,905-110,966,276 , GRCh38.p12 chr13: 110,313,558-110,313,929 COL4A2
    nsv6121974copy number variation1nstd186human GRCh37 chr13: 111,037,746-111,038,410 , GRCh38.p12 chr13: 110,385,399-110,386,063 COL4A2
    nsv5980390copy number variation1nstd102humanUncertain significance GRCh37 chr13: 110,802,791-110,959,290 , GRCh38.p12 chr13: 110,150,444-110,306,943 COL4A1, COL4A2
    nsv5978178insertion1nstd209human GRCh38 chr13: 110,477,526-110,477,526 , GRCh37.p13 chr13: 111,129,873-111,129,873 COL4A2
    nsv5977555insertion1nstd209human GRCh38 chr13: 110,424,448-110,424,448 , GRCh37.p13 chr13: 111,076,795-111,076,795 COL4A2
    nsv5970607insertion1nstd209human GRCh38 chr13: 110,432,499-110,432,499 , GRCh37.p13 chr13: 111,084,846-111,084,846 COL4A2
    nsv5947513copy number variation1nstd209human GRCh38 chr13: 110,385,410-110,385,769 , GRCh37.p13 chr13: 111,037,757-111,038,116 COL4A2
    nsv5946104copy number variation1nstd209human GRCh38 chr13: 110,496,525-110,497,290 , GRCh37.p13 chr13: 111,148,872-111,149,637 COL4A2
    nsv5945379copy number variation1nstd209human GRCh38 chr13: 110,380,666-110,380,725 , GRCh37.p13 chr13: 111,033,013-111,033,072 COL4A2
    nsv5945053copy number variation1nstd209human GRCh38 chr13: 110,408,835-110,408,985 , GRCh37.p13 chr13: 111,061,182-111,061,332 COL4A2
    nsv5944459copy number variation1nstd209human GRCh38 chr13: 110,481,742-110,482,007 , GRCh37.p13 chr13: 111,134,089-111,134,354 COL4A2
    nsv5942480copy number variation1nstd209human GRCh38 chr13: 110,409,110-110,409,183 , GRCh37.p13 chr13: 111,061,457-111,061,530 COL4A2
    nsv5941549copy number variation1nstd209human GRCh38 chr13: 110,496,522-110,496,693 , GRCh37.p13 chr13: 111,148,869-111,149,040 COL4A2
    nsv5941039copy number variation1nstd209human GRCh38 chr13: 110,340,170-110,340,342 , GRCh37.p13 chr13: 110,992,517-110,992,689 MIR8073, COL4A2
    nsv5940371copy number variation1nstd209human GRCh38 chr13: 110,496,993-110,498,036 , GRCh37.p13 chr13: 111,149,340-111,150,383 COL4A2
    nsv5934986copy number variation1nstd209human GRCh38 chr13: 110,410,722-110,411,957 , GRCh37.p13 chr13: 111,063,069-111,064,304 COL4A2
    nsv5934306copy number variation1nstd209human GRCh38 chr13: 110,313,535-110,313,840 , GRCh37.p13 chr13: 110,965,882-110,966,187 COL4A2
    nsv5933807copy number variation1nstd209human GRCh38 chr13: 110,483,680-110,483,729 , GRCh37.p13 chr13: 111,136,027-111,136,076 COL4A2
    nsv5931607copy number variation1nstd209human GRCh38 chr13: 110,497,275-110,497,574 , GRCh37.p13 chr13: 111,149,622-111,149,921 COL4A2
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