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Items: 1 to 20 of 38

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3971740copy number variation1nstd102humanLikely benign GRCh37 chr1: 217,748,650-217,893,701 , GRCh38.p12 chr1: 217,575,308-217,720,359 GPATCH2, SPATA17
    nsv3896513copy number variation1nstd102humanPathogenic NCBI36 chr1: 214,636,660-215,789,771 , GRCh37 chr1: 216,570,037-217,723,148 , GRCh38 chr1: 216,396,695-217,549,806 GPATCH2, ESRRG, 4 more genes
    nsv6290569copy number variation1nstd102humanPathogenic GRCh37 chr1: 215,199,578-223,035,427 , GRCh38.p12 chr1: 215,026,235-222,862,085 GPATCH2, SPATA17, 97 more genes
    nsv3898157copy number variation2nstd102humanPathogenic NCBI36 chr1: 213,446,726-220,244,033 , GRCh38 chr1: 215,206,760-222,004,068 , GRCh37 chr1: 215,380,103-222,177,410 GPATCH2, LINC01352, 79 more genes
    nsv1398588copy number variation1nstd102humanPathogenic GRCh37 chr1: 215,588,712-222,145,072 , GRCh38.p12 chr1: 215,415,369-221,971,730 GPATCH2, RPS26P17, 77 more genes
    nsv6290612copy number variation1nstd102humanPathogenic GRCh37 chr1: 216,243,817-220,231,236 , GRCh38.p12 chr1: 216,070,475-220,057,894 GPATCH2, LINC00210, 36 more genes
    nsv1398641copy number variation1nstd102humanPathogenic GRCh37 chr1: 216,672,181-220,202,575 , GRCh38.p12 chr1: 216,498,839-220,029,233 GPATCH2, TGFB2-AS1, 30 more genes
    nsv3888593copy number variation1nstd102humanPathogenic GRCh37 chr1: 215,829,463-219,225,857 , GRCh38.p12 chr1: 215,656,121-219,052,515 GPATCH2, LINC01710, 24 more genes
    nsv3901095copy number variation1nstd102humanPathogenic NCBI36 chr1: 214,758,572-218,067,255 , GRCh38 chr1: 216,518,607-219,827,290 , GRCh37 chr1: 216,691,949-220,000,632 GPATCH2, NXNP1, 27 more genes
    nsv6290478copy number variation1nstd102humanPathogenic GRCh37 chr1: 217,219,510-219,385,296 , GRCh38.p12 chr1: 217,046,168-219,211,954 GPATCH2, ESRRG, 22 more genes
    nsv6290633copy number variation1nstd102humanPathogenic GRCh37 chr1: 217,589,671-219,026,274 , GRCh38.p12 chr1: 217,416,329-218,852,932 GPATCH2, LINC01653, 15 more genes
    nsv3909598copy number variation1nstd102humanPathogenic GRCh38 chr1: 217,452,423-218,818,361 , GRCh37 chr1: 217,625,765-218,991,703 , NCBI36 chr1: 215,692,388-217,058,326 GPATCH2, RNU1-141P, 14 more genes
    nsv3878193copy number variation1nstd102humanPathogenic GRCh37 chr1: 217,699,328-218,689,648 , GRCh38.p12 chr1: 217,525,986-218,516,306 GPATCH2, LOC105372922, 13 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 GPATCH2, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 GPATCH2, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 GPATCH2, 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 GPATCH2, RGS18, 1186 more genes
    nsv3881012copy number variation1nstd102humanPathogenic GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801 GPATCH2, LOC105372928, 1062 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 GPATCH2, LOC105373279, 1036 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 GPATCH2, RNA5S8, 893 more genes
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