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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3880733copy number variation1nstd102humanLikely benign GRCh37 chr1: 204,974,667-205,046,024 , GRCh38.p12 chr1: 205,005,539-205,076,896 NFASC, CNTN2
    nsv3885651copy number variation1nstd102humanUncertain significance GRCh37 chr1: 204,907,784-205,052,260 , GRCh38.p12 chr1: 204,938,656-205,083,132 NFASC, RPL13AP11, 2 more genes
    nsv3877577copy number variation1nstd102humanconflicting data from submitters GRCh37 chr1: 204,907,784-205,027,918 , GRCh38.p12 chr1: 204,938,656-205,058,790 NFASC, CNTN2, 1 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 NFASC, CRB1, 1608 more genes
    nsv3881313copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,682,513-212,815,646 , GRCh38.p12 chr1: 204,713,385-212,642,304 NFASC, IL19, 184 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 NFASC, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 NFASC, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 NFASC, RNU1-153P, 4887 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 NFASC, LOC101060227, 1608 more genes
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 NFASC, RGS18, 1186 more genes
    nsv3881012copy number variation1nstd102humanPathogenic GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801 NFASC, LOC105372928, 1062 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 NFASC, LOC105373279, 1036 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 NFASC, 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 NFASC, LOC107985458, 590 more genes
    nsv3889347copy number variation1nstd102humanPathogenic GRCh37 chr1: 185,644,663-221,698,833 , GRCh38.p12 chr1: 185,675,531-221,525,491 NFASC, MIR1231, 543 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 NFASC, PRELP, 527 more genes
    nsv3879807copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,811,907-228,997,888 , GRCh38.p12 chr1: 197,842,777-228,862,141 NFASC, 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 NFASC, HLX, 354 more genes
    nsv3877139copy number variation1nstd102humanLikely pathogenic GRCh38 chr1: 204,033,173-208,209,798 , GRCh37.p13 chr1: 204,002,301-208,383,143 NFASC, AVPR1B, 120 more genes
    nsv4674816copy number variation1nstd102humanUncertain significance GRCh37 chr1: 204,954,317-205,346,803 , GRCh38.p12 chr1: 204,985,189-205,377,675 NFASC, CNTN2, 12 more genes
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