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    Number of Variants: 10

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv884822copy number variation2547nstd71human NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715 HLA-DRB5
    nsv909839copy number variation966nstd71human NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591 CCDC102B
    nsv884201copy number variation3nstd71human NCBI36 chr6: 31,384,589-31,401,219 , GRCh37.p13 chr6|NT_167249.1: 2,610,355-2,626,958 , GRCh37.p13 chr6: 31,276,610-31,293,240 , GRCh38.p12 chr6: 31,308,833-31,325,463 , GRCh38.p12 chr6|NT_167249.2: 2,611,057-2,627,660 LOC112267902
    nsv903647copy number variation13nstd71human NCBI36 chr15: 21,985,041-22,096,612 , GRCh37.p13 chr15: 24,433,948-24,545,519 , GRCh38.p12 chr15: 24,188,801-24,300,372 LOC105370733, LOC105370732
    nsv895761copy number variation319nstd71human NCBI36 chr10: 81,462,715-81,497,813 , GRCh37.p13 chr10: 81,472,521-81,507,631 , GRCh38.p12 chr10: 79,712,765-79,747,875 NUTM2B, NUTM2B-AS1
    nsv914690copy number variation1nstd71human NCBI36 chr22: 23,991,725-24,163,596 , GRCh37.p13 chr22: 25,661,725-25,833,596 , GRCh38.p12 chr22: 25,265,758-25,437,629 IGLL3P, LOC105372969, 2 more genes
    nsv879310copy number variation1929nstd71human NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558 LOC100422402, LOC100132651, 2 more genes
    nsv907853copy number variation28nstd71human NCBI36 chr17: 18,971,335-19,040,640 , GRCh37.p13 chr17: 19,030,610-19,100,047 , GRCh38.p12 chr17: 19,127,297-19,196,734 SNORD3C, GRAPL-AS1, 3 more genes
    nsv883917copy number variation2nstd71human NCBI36 chr6: 29,988,619-30,004,400 , GRCh37.p13 chr6|NT_167246.1: 1,174,816-1,190,626 , GRCh37.p13 chr6: 29,880,640-29,896,421 , GRCh38.p12 chr6|NT_167246.2: 1,169,196-1,185,006 , GRCh38.p12 chr6: 29,912,863-29,928,644 HLA-K, HCG4B, 1 more genes
    nsv914901copy number variation2nstd71human NCBI36 chr22: 24,198,241-24,235,668 , GRCh37.p13 chr22: 25,868,241-25,905,668 , GRCh38.p12 chr22: 25,472,274-25,509,701 0
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