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Items: 1 to 20 of 27

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3872981copy number variation1nstd102humanBenign GRCh37 chr1: 207,288,297-207,293,178 , GRCh38.p12 chr1: 207,114,952-207,119,833 C4BPA
    nsv3884632copy number variation1nstd102humanBenign GRCh37 chr1: 207,289,436-207,293,178 , GRCh38.p12 chr1: 207,116,091-207,119,833 C4BPA
    nsv3875785copy number variation1nstd102humanBenign GRCh37 chr1: 207,291,126-207,293,496 , GRCh38.p12 chr1: 207,117,781-207,120,151 C4BPA
    nsv3873893copy number variation1nstd102humanBenign GRCh37 chr1: 207,291,126-207,293,173 , GRCh38.p12 chr1: 207,117,781-207,119,828 C4BPA
    nsv3885780copy number variation1nstd102humanBenign GRCh37 chr1: 207,292,616-207,293,496 , GRCh38.p12 chr1: 207,119,271-207,120,151 C4BPA
    nsv3874764copy number variation1nstd102humanBenign GRCh37 chr1: 207,292,578-207,293,178 , GRCh38.p12 chr1: 207,119,233-207,119,833 C4BPA
    nsv3886861copy number variation1nstd102humanBenign GRCh37 chr1: 207,292,578-207,293,173 , GRCh38.p12 chr1: 207,119,233-207,119,828 C4BPA
    nsv3881313copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,682,513-212,815,646 , GRCh38.p12 chr1: 204,713,385-212,642,304 C4BPA, IL19, 184 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 C4BPA, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 C4BPA, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 C4BPA, RNU1-153P, 4887 more genes
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 C4BPA, RGS18, 1186 more genes
    nsv3881012copy number variation1nstd102humanPathogenic GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801 C4BPA, LOC105372928, 1062 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 C4BPA, LOC105373279, 1036 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 C4BPA, RNA5S8, 893 more genes
    nsv3895767copy number variation1nstd102humanPathogenic GRCh38 chr1: 187,143,981-224,299,417 , NCBI36 chr1: 185,379,736-222,553,742 , GRCh37 chr1: 187,113,113-224,487,119 C4BPA, LOC107985458, 590 more genes
    nsv3889347copy number variation1nstd102humanPathogenic GRCh37 chr1: 185,644,663-221,698,833 , GRCh38.p12 chr1: 185,675,531-221,525,491 C4BPA, MIR1231, 543 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 C4BPA, PRELP, 527 more genes
    nsv3879807copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,811,907-228,997,888 , GRCh38.p12 chr1: 197,842,777-228,862,141 C4BPA, RABIF, 637 more genes
    nsv3892738copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,734,042-225,596,400 , NCBI36 chr1: 203,000,665-223,663,023 , GRCh38 chr1: 204,764,914-225,408,698 C4BPA, HLX, 354 more genes
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