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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7093375copy number variation1nstd102humannot provided GRCh37 chr1: 217,923,165-218,542,059 , GRCh38.p12 chr1: 217,749,823-218,368,717 LINC01653, LINC00210, 10 more genes
    nsv6672724copy number variation1nstd229human GRCh38 chr1: 217,803,608-217,849,902 , GRCh37.p13 chr1: 217,976,950-218,023,244 UBBP2, SPATA17
    nsv6670037copy number variation1nstd229human GRCh38 chr1: 217,814,587-218,303,167 , GRCh37.p13 chr1: 217,987,929-218,476,509 UBBP2, LINC01653, 6 more genes
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6327163copy number variation1nstd223human GRCh38 chr1: 217,814,587-218,303,167 , GRCh37.p13 chr1: 217,987,929-218,476,509 SPATA17, LINC01653, 6 more genes
    nsv6313524copy number variation1nstd102humanUncertain significance GRCh37 chr1: 216,767,549-218,152,575 , GRCh38.p12 chr1: 216,594,207-217,979,233 SPATA17, LINC00210, 7 more genes
    nsv6290633copy number variation1nstd102humanPathogenic GRCh37 chr1: 217,589,671-219,026,274 , GRCh38.p12 chr1: 217,416,329-218,852,932 LINC01653, SPATA17-AS1, 15 more genes
    nsv6290612copy number variation1nstd102humanPathogenic GRCh37 chr1: 216,243,817-220,231,236 , GRCh38.p12 chr1: 216,070,475-220,057,894 LINC00210, LOC107985281, 36 more genes
    nsv6290569copy number variation1nstd102humanPathogenic GRCh37 chr1: 215,199,578-223,035,427 , GRCh38.p12 chr1: 215,026,235-222,862,085 SPATA17, BROX, 97 more genes
    nsv6290478copy number variation1nstd102humanPathogenic GRCh37 chr1: 217,219,510-219,385,296 , GRCh38.p12 chr1: 217,046,168-219,211,954 ESRRG, TGFB2, 22 more genes
    nsv6133857copy number variation1nstd213human GRCh37 chr1: 215,920,000-223,130,001 , GRCh38.p12 chr1: 215,746,658-222,956,659 BPNT1, HHIPL2, 95 more genes
    nsv6133757copy number variation1nstd213human GRCh37 chr1: 217,950,000-218,650,001 , GRCh38.p12 chr1: 217,776,658-218,476,659 SPATA17, LINC01653, 11 more genes
    nsv6133756copy number variation1nstd213human GRCh37 chr1: 216,560,000-218,080,001 , GRCh38.p12 chr1: 216,386,658-217,906,659 SPATA17, LOC105372920, 8 more genes
    nsv6133630copy number variation2nstd213human GRCh37 chr1: 206,490,000-223,720,001 , GRCh38.p12 chr1: 206,316,655-223,546,636 ATP5MC2P1, CENPF, 269 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4904355copy number variation1nstd200human GRCh38 chr1: 217,814,587-218,303,169 , GRCh37.p13 chr1: 217,987,929-218,476,511 SPATA17, LINC01653, 6 more genes
    nsv4781451copy number variation1nstd200human GRCh37 chr1: 217,987,929-218,476,511 , GRCh38.p12 chr1: 217,814,587-218,303,169 SPATA17, LINC01653, 6 more genes
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