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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5871405copy number variation1nstd209human GRCh38 chr1: 32,018,418-32,018,713 , GRCh37.p13 chr1: 32,484,019-32,484,314 KHDRBS1
    nsv5829694copy number variation1nstd209human GRCh38 chr1: 32,054,585-32,056,084 , GRCh37.p13 chr1: 32,520,186-32,521,685 KHDRBS1
    nsv5380686translocation1nstd200human GRCh38 chr1: 32,006,917-32,006,917 , GRCh38 chr1: 32,012,288-32,012,288 , GRCh37.p13 chr1: 32,472,518-32,472,518 , GRCh37.p13 chr1: 32,477,889-32,477,889 KHDRBS1
    nsv5361099translocation1nstd200human GRCh38 chr1: 32,014,377-32,014,377 , GRCh38 chr1: 32,030,294-32,030,294 , GRCh37.p13 chr1: 32,479,978-32,479,978 , GRCh37.p13 chr1: 32,495,895-32,495,895 KHDRBS1
    nsv5291467copy number variation1nstd204human GRCh38.p13 chr1: 32,049,052-32,064,673 , GRCh37.p13 chr1: 32,514,653-32,530,274 KHDRBS1
    nsv5218645copy number variation1nstd204human GRCh38.p13 chr1: 32,049,101-32,064,700 , GRCh37.p13 chr1: 32,514,702-32,530,301 KHDRBS1
    nsv5213456copy number variation1nstd204human GRCh38.p13 chr1: 31,802,501-32,105,200 , GRCh37.p13 chr1: 32,268,102-32,570,801 TMEM39B, KHDRBS1, 3 more genes
    nsv5212402copy number variation1nstd204human GRCh38.p13 chr1: 32,048,977-32,064,579 , GRCh37.p13 chr1: 32,514,578-32,530,180 KHDRBS1
    nsv5206341copy number variation1nstd204human GRCh38.p13 chr1: 32,055,485-32,057,184 , GRCh37.p13 chr1: 32,521,086-32,522,785 KHDRBS1
    nsv5068408mobile element insertion1nstd203human GRCh38 chr1: 32,022,553-32,022,564 , GRCh37.p13 chr1: 32,488,154-32,488,165 KHDRBS1
    nsv4903320copy number variation1nstd200human GRCh38 chr1: 32,049,054-32,049,811 , GRCh37.p13 chr1: 32,514,655-32,515,412 KHDRBS1
    nsv4895796copy number variation1nstd200human GRCh38 chr1: 32,055,297-32,057,947 , GRCh37.p13 chr1: 32,520,898-32,523,548 KHDRBS1
    nsv4895795copy number variation1nstd200human GRCh38 chr1: 32,047,321-32,049,736 , GRCh37.p13 chr1: 32,512,922-32,515,337 KHDRBS1
    nsv4895794copy number variation1nstd200human GRCh38 chr1: 32,047,525-32,047,617 , GRCh37.p13 chr1: 32,513,126-32,513,218 KHDRBS1
    nsv4895793copy number variation1nstd200human GRCh38 chr1: 32,029,174-32,030,285 , GRCh37.p13 chr1: 32,494,775-32,495,886 KHDRBS1
    nsv4895792copy number variation1nstd200human GRCh38 chr1: 32,017,931-32,019,407 , GRCh37.p13 chr1: 32,483,532-32,485,008 KHDRBS1
    nsv4895791copy number variation1nstd200human GRCh38 chr1: 32,017,022-32,017,877 , GRCh37.p13 chr1: 32,482,623-32,483,478 KHDRBS1
    nsv4895790copy number variation1nstd200human GRCh38 chr1: 32,015,945-32,017,130 , GRCh37.p13 chr1: 32,481,546-32,482,731 KHDRBS1
    nsv4895789copy number variation1nstd200human GRCh38 chr1: 32,004,175-32,011,889 , GRCh37.p13 chr1: 32,469,776-32,477,490 KHDRBS1
    nsv4772953copy number variation1nstd200human GRCh37 chr1: 32,494,775-32,495,886 , GRCh38.p12 chr1: 32,029,174-32,030,285 KHDRBS1
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