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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3921757copy number variation1nstd102humannot provided NCBI36 chr1: 214,401,568-247,249,719 , GRCh37.p13 chr1: 216,334,945-249,233,096 , GRCh38.p12 chr1: 216,161,603-248,938,897 MTCYBP15, RNU4-77P, 658 more genes
    nsv3914847copy number variation1nstd102humanPathogenic NCBI36 chr1: 223,116,610-247,199,719 , GRCh37.p13 chr1: 225,049,987-249,233,096 , GRCh38.p12 chr1: 224,862,285-248,938,897 RNU6-1089P, TRE-CTC2-1, 518 more genes
    nsv3907781copy number variation1nstd102humanUncertain significance NCBI36 chr1: 228,086,175-229,719,922 , GRCh37 chr1: 230,019,552-231,653,299 , GRCh38 chr1: 229,883,805-231,517,553 TTC13, AGT, 34 more genes
    nsv3907533copy number variation2nstd102humanUncertain significance GRCh38 chr1: 230,519,755-231,232,066 , NCBI36 chr1: 228,722,124-229,434,435 , GRCh37 chr1: 230,655,501-231,367,812 RPS24P4, LOC107985358, 21 more genes
    nsv3906964copy number variation1nstd102humanPathogenic GRCh37 chr1: 224,075,482-249,185,508 , NCBI36 chr1: 222,142,105-247,152,131 , GRCh38 chr1: 223,887,780-248,891,309 KIF26B, RPSAP21, 542 more genes
    nsv3905747copy number variation1nstd102humanUncertain significance GRCh38 chr1: 230,489,657-231,243,203 , GRCh37 chr1: 230,625,403-231,378,949 , NCBI36 chr1: 228,692,026-229,445,572 LOC101927604, MIR1182, 23 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 MIR3123, LOC100506929, 221 more genes
    nsv3903290copy number variation1nstd102humanPathogenic GRCh38 chr1: 223,815,147-248,918,469 , NCBI36 chr1: 222,069,472-247,179,291 , GRCh37 chr1: 224,002,849-249,212,668 RNA5S12, OR2T27, 546 more genes
    nsv3902226copy number variation1nstd102humanPathogenic NCBI36 chr1: 221,587,658-247,179,291 , GRCh37 chr1: 223,521,035-249,212,668 , GRCh38 chr1: 223,347,693-248,918,469 TFB2M, IBA57, 558 more genes
    nsv3901864copy number variation1nstd102humanPathogenic NCBI36 chr1: 227,225,279-247,179,291 , GRCh37 chr1: 229,158,656-249,212,668 , GRCh38 chr1: 229,022,909-248,918,469 OR2T33, MTCYBP15, 396 more genes
    nsv3901721copy number variation1nstd102humanPathogenic GRCh38 chr1: 224,022,862-248,918,469 , NCBI36 chr1: 222,277,187-247,179,291 , GRCh37 chr1: 224,210,564-249,212,668 RNU6-947P, RNA5SP80, 539 more genes
    nsv3900253copy number variation1nstd102humanUncertain significance NCBI36 chr1: 228,951,700-229,394,926 , GRCh37 chr1: 230,885,077-231,328,303 , GRCh38 chr1: 230,749,331-231,192,557 LOC644006, C1orf198, 13 more genes
    nsv3899586copy number variation1nstd102humanPathogenic NCBI36 chr1: 222,082,825-247,152,131 , GRCh37 chr1: 224,016,202-249,185,508 , GRCh38 chr1: 223,828,500-248,891,309 ENAH, CIAO2AP2, 545 more genes
    nsv3899452copy number variation1nstd102humanPathogenic NCBI36 chr1: 224,439,448-231,074,857 , GRCh37 chr1: 226,372,825-233,008,234 , GRCh38 chr1: 226,185,124-232,872,488 RNA5S10, SIPA1L2, 178 more genes
    nsv3898777copy number variation1nstd102humanPathogenic NCBI36 chr1: 223,692,805-247,048,022 , GRCh38 chr1: 225,438,480-248,787,200 , GRCh37 chr1: 225,626,182-249,060,210 LOC105373258, LOC100129949, 506 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 RPS18P3, LOC128136, 793 more genes
    nsv3893960copy number variation1nstd102humanPathogenic NCBI36 chr1: 222,350,813-247,179,291 , GRCh37 chr1: 224,284,190-249,212,668 , GRCh38 chr1: 224,096,488-248,918,469 CDKN2AIPNLP1, LOC105373215, 537 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 LOC105373046, MIR4677, 740 more genes
    nsv3892503copy number variation1nstd102humanPathogenic NCBI36 chr1: 212,263,778-247,179,291 , GRCh38 chr1: 214,023,812-248,918,469 , GRCh37 chr1: 214,197,155-249,212,668 HMGN2P19, RNA5S2, 672 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 HLX, LOC107985281, 749 more genes
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