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Items: 1 to 20 of 345

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148271copy number variation1nstd102humanPathogenic GRCh38 chr18: 158,286-14,124,574 , GRCh37.p13 chr18: 158,286-14,124,573 PMM2P2, EIF4A2P1, 225 more genes
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7075587inversion1nstd229human GRCh38 chr18: 499,678-1,806,279 , GRCh37.p13 chr18: 499,678-1,806,280 LOC105371954, COLEC12, 23 more genes
    nsv7073472inversion1nstd229human GRCh38 chr18: 923,429-984,825 , GRCh37.p13 chr18: 923,430-984,826 LOC107985165, LINC01904
    nsv7072148inversion1nstd229human GRCh38 chr18: 906,157-1,334,760 , GRCh37.p13 chr18: 906,158-1,334,761 ADCYAP1, LINC00470, 6 more genes
    nsv7070144inversion1nstd229human GRCh38 chr18: 599,101-1,058,089 , GRCh37.p13 chr18: 599,101-1,058,090 LOC105371952, TYMSOS, 10 more genes
    nsv7069227inversion1nstd229human GRCh38 chr18: 305,918-1,971,959 , GRCh37.p13 chr18: 305,918-1,971,960 LOC105371960, CLUL1, 26 more genes
    nsv7067747inversion1nstd229human GRCh38 chr18: 844,123-1,800,732 , GRCh37.p13 chr18: 844,124-1,800,733 LINC01904, LOC105371959, 11 more genes
    nsv7059777inversion1nstd229human GRCh38 chr18: 712,529-1,045,946 , GRCh37.p13 chr18: 712,529-1,045,947 ENOSF1, BOLA2P1, 6 more genes
    nsv7059342inversion1nstd229human GRCh38 chr18: 457,327-1,560,638 , GRCh37.p13 chr18: 457,327-1,560,639 RNU1-109P, CETN1, 22 more genes
    nsv6997549copy number variation1nstd229human GRCh38 chr18: 914,277-926,110 , GRCh37.p13 chr18: 914,278-926,111 LINC01904
    nsv6996744copy number variation1nstd229human GRCh38 chr18: 565,501-1,482,500 , GRCh37.p13 chr18: 565,501-1,482,501 LOC441806, LOC105371953, 19 more genes
    nsv6992627copy number variation1nstd229human GRCh38 chr18: 928,301-941,900 , GRCh37.p13 chr18: 928,302-941,901 LINC01904
    nsv6986693copy number variation1nstd229human GRCh38 chr18: 707,824-987,436 , GRCh37.p13 chr18: 707,824-987,437 LOC441806, ENOSF1, 6 more genes
    nsv6983512copy number variation1nstd229human GRCh38 chr18: 702,287-994,311 , GRCh37.p13 chr18: 702,287-994,312 YES1, ADCYAP1, 6 more genes
    nsv6982600copy number variation1nstd229human GRCh38 chr18: 927,006-938,392 , GRCh37.p13 chr18: 927,007-938,393 LINC01904
    nsv6980773copy number variation1nstd229human GRCh38 chr18: 745,078-937,101 , GRCh37.p13 chr18: 745,078-937,102 BOLA2P1, RNU1-109P, 4 more genes
    nsv6980010copy number variation1nstd229human GRCh38 chr18: 780,775-925,407 , GRCh37.p13 chr18: 780,776-925,408 YES1, LINC01904, 4 more genes
    nsv6637580copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-7,218,594 , GRCh38.p12 chr18: 136,227-7,218,596 L3MBTL4-AS1, LOC101927044, 106 more genes
    nsv6637296copy number variation1nstd102humanUncertain significance GRCh37 chr18: 136,227-2,626,840 , GRCh38.p12 chr18: 136,227-2,626,841 LOC105371953, LOC105371959, 36 more genes
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