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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
    nsv7093065copy number variation1nstd102humanUncertain significance GRCh38 chr1: 220,136,865-220,136,866 , GRCh37 chr1: 220,310,207-220,310,208 IARS2
    nsv6310857copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,320,815-220,320,977 , GRCh38.p12 chr1: 220,147,473-220,147,635 IARS2, RAB3GAP2
    nsv7096026copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,298,559-220,325,126 , GRCh38.p12 chr1: 220,125,217-220,151,784 IARS2, RAB3GAP2, 1 more genes
    nsv6290569copy number variation1nstd102humanPathogenic GRCh37 chr1: 215,199,578-223,035,427 , GRCh38.p12 chr1: 215,026,235-222,862,085 IARS2, 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 IARS2, LINC01352, 79 more genes
    nsv1398588copy number variation1nstd102humanPathogenic GRCh37 chr1: 215,588,712-222,145,072 , GRCh38.p12 chr1: 215,415,369-221,971,730 IARS2, RPS26P17, 77 more genes
    nsv4674721copy number variation1nstd102humanPathogenic GRCh37 chr1: 219,734,913-224,104,993 , GRCh38.p12 chr1: 219,561,571-223,917,291 IARS2, PRELID3BP1, 82 more genes
    nsv7095972copy number variation1nstd102humanPathogenic GRCh37 chr1: 218,520,044-220,986,760 , GRCh38.p12 chr1: 218,346,702-220,813,418 IARS2, TGFB2, 38 more genes
    nsv7095973copy number variation1nstd102humanPathogenic GRCh37 chr1: 220,088,791-220,445,679 , GRCh38.p12 chr1: 219,915,449-220,272,337 IARS2, AURKAP1, 13 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 IARS2, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 IARS2, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 IARS2, 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 IARS2, RGS18, 1186 more genes
    nsv3881012copy number variation1nstd102humanPathogenic GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801 IARS2, LOC105372928, 1062 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 IARS2, LOC105373279, 1036 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 IARS2, RNA5S8, 893 more genes
    nsv3897747copy number variation1nstd102humanPathogenic GRCh38 chr1: 207,346,642-248,930,485 , GRCh37 chr1: 207,519,987-249,224,684 , NCBI36 chr1: 205,586,610-247,191,307 IARS2, RPS18P3, 793 more genes
    nsv3890682copy number variation1nstd102humanPathogenic GRCh37 chr1: 209,819,552-249,225,312 , NCBI36 chr1: 207,886,175-247,191,935 , GRCh38 chr1: 209,646,207-248,931,113 IARS2, HLX, 749 more genes
    nsv3892818copy number variation1nstd102humanPathogenic GRCh38 chr1: 209,963,625-248,918,469 , GRCh37 chr1: 210,136,970-249,212,668 , NCBI36 chr1: 208,203,593-247,179,291 IARS2, LOC105373046, 740 more genes
    nsv4684187copy number variation1nstd102humanPathogenic GRCh37 chr1: 210,152,794-249,218,992 , GRCh38.p12 chr1: 209,979,449-248,924,793 IARS2, HLX-AS1, 740 more genes
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