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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883736copy number variation1nstd102humanLikely benign GRCh37 chr1: 233,688,767-233,967,082 , GRCh38.p12 chr1: 233,553,021-233,831,336 KCNK1, MIR4427, 1 more genes
    nsv4453122copy number variation1nstd102humanUncertain significance GRCh37 chr1: 233,514,111-233,998,612 , GRCh38.p12 chr1: 233,378,365-233,862,866 KCNK1, MAP3K21, 3 more genes
    nsv6634337copy number variation1nstd102humanPathogenic GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719 KCNK1, OR2M4, 316 more genes
    nsv3904200copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,106,271-243,677,283 , NCBI36 chr1: 228,308,641-241,907,208 , GRCh37 chr1: 230,242,018-243,840,585 KCNK1, MIR3123, 221 more genes
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 KCNK1, AGT, 221 more genes
    nsv4674115copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,653,722-234,591,807 , GRCh38.p12 chr1: 223,480,380-234,456,061 KCNK1, LOC105373163, 258 more genes
    nsv6636217copy number variation1nstd102humanPathogenic GRCh37 chr1: 232,732,121-243,338,216 , GRCh38.p12 chr1: 232,596,375-243,174,914 KCNK1, LINC01347, 169 more genes
    nsv3912845copy number variation1nstd102humanPathogenic NCBI36 chr1: 230,713,047-240,722,962 , GRCh37.p13 chr1: 232,646,424-242,656,339 , GRCh38.p12 chr1: 232,510,678-242,493,037 KCNK1, RNU4-77P, 158 more genes
    nsv3881799copy number variation1nstd102humanPathogenic GRCh37 chr1: 232,226,609-241,010,904 , GRCh38.p12 chr1: 232,090,863-240,847,604 KCNK1, MIPEPP2, 137 more genes
    nsv6112661copy number variation1nstd102humanPathogenic GRCh37 chr1: 231,407,943-237,289,859 , GRCh38.p12 chr1: 231,272,197-237,126,559 KCNK1, LOC105373207, 113 more genes
    nsv7137173copy number variation1nstd102humanPathogenic GRCh38 chr1: 233,502,994-236,105,019 , GRCh37.p13 chr1: 233,638,740-236,268,319 KCNK1, ARID4B, 58 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 KCNK1, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 KCNK1, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 KCNK1, 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 KCNK1, RGS18, 1186 more genes
    nsv3881012copy number variation1nstd102humanPathogenic GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801 KCNK1, LOC105372928, 1062 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 KCNK1, LOC105373279, 1036 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 KCNK1, 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 KCNK1, 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 KCNK1, HLX, 749 more genes
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