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Items: 1 to 20 of 171

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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
    nsv7040987inversion1nstd229human GRCh38 chr1: 210,564,176-212,658,793 , GRCh37.p13 chr1: 210,737,520-212,832,135 LPGAT1, RFKP5, 44 more genes
    nsv6677944copy number variation1nstd229human GRCh38 chr1: 212,442,839-212,444,128 , GRCh37.p13 chr1: 212,616,181-212,617,470 NENF
    nsv6677817copy number variation1nstd229human GRCh38 chr1: 212,446,749-212,451,168 , GRCh37.p13 chr1: 212,620,091-212,624,510 NENF
    nsv6674297copy number variation1nstd229human GRCh38 chr1: 212,438,255-212,440,951 , GRCh37.p13 chr1: 212,611,597-212,614,293 NENF
    nsv6672344copy number variation1nstd229human GRCh38 chr1: 212,446,679-212,468,419 , GRCh37.p13 chr1: 212,620,021-212,641,761 NENF, LINC02771
    nsv6658648copy number variation1nstd229human GRCh38 chr1: 212,405,926-212,437,938 , GRCh37.p13 chr1: 212,579,268-212,611,280 NENF, LOC105372906, 1 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
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 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
    nsv6328970copy number variation1nstd223human GRCh38 chr1: 212,432,701-212,433,200 , GRCh37.p13 chr1: 212,606,043-212,606,542 LOC105372906, NENF
    nsv6327339copy number variation1nstd223human GRCh38 chr1: 212,442,838-212,444,126 , GRCh37.p13 chr1: 212,616,180-212,617,468 NENF
    nsv6326622copy number variation1nstd223human GRCh38 chr1: 212,435,564-212,436,306 , GRCh37.p13 chr1: 212,608,906-212,609,648 NENF
    nsv6325553copy number variation1nstd223human GRCh38 chr1: 209,453,567-212,914,449 , GRCh37.p13 chr1: 209,626,912-213,087,791 ST13P19, RPS5P4, 74 more genes
    nsv6321078copy number variation1nstd223human GRCh38 chr1: 212,439,561-212,440,179 , GRCh37.p13 chr1: 212,612,903-212,613,521 NENF
    nsv6291634copy number variation1nstd102humanUncertain significance GRCh38 chr1: 212,337,801-213,362,035 , GRCh37.p13 chr1: 212,511,143-213,535,378 ANGEL2, ATF3, 21 more genes
    nsv6133848copy number variation1nstd213human GRCh37 chr1: 212,280,000-213,040,001 , GRCh38.p12 chr1: 212,106,658-212,866,659 NENF, GARIN4, 20 more genes
    nsv6133754copy number variation1nstd213human GRCh37 chr1: 212,010,000-212,890,001 , GRCh38.p12 chr1: 211,836,658-212,716,659 PPP2R5A, PACC1, 19 more genes
    nsv6133753copy number variation1nstd213human GRCh37 chr1: 210,410,000-214,880,001 , GRCh38.p12 chr1: 210,236,655-214,706,658 NEK2, PPP2R5A, 73 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
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