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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096310copy number variation1nstd102humanPathogenic GRCh37 chr22: 38,097,373-39,306,081 , GRCh38.p12 chr22: 37,701,366-38,910,076 TMEM184B, ANKRD54, 46 more genes
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7095836copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 37,154,355-39,148,633 , GRCh38.p12 chr22: 36,758,311-38,752,628 CSF2RBP1, H1-0, 80 more genes
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7073136inversion1nstd229human GRCh38 chr22: 37,870,298-37,898,164 , GRCh37.p13 chr22: 38,266,305-38,294,171 EIF3L, RNU6-900P
    nsv7072766inversion1nstd229human GRCh38 chr22: 35,603,617-39,341,195 , GRCh37.p13 chr22: 35,999,664-39,737,200 APOL5, MTATP6P20, 132 more genes
    nsv7067151inversion1nstd229human GRCh38 chr22: 37,862,494-37,904,603 , GRCh37.p13 chr22: 38,258,501-38,300,610 RNU6-900P, EIF3L, 1 more genes
    nsv7064066inversion1nstd229human GRCh38 chr22: 34,920,312-39,418,308 , GRCh37.p13 chr22: 35,316,302-39,814,313 LOC112268295, APOBEC3B-AS1, 150 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7059210inversion1nstd229human GRCh38 chr22: 35,603,611-39,337,136 , GRCh37.p13 chr22: 35,999,658-39,733,141 MTCO2P20, RPS29P31, 132 more genes
    nsv7037127copy number variation1nstd229human GRCh38 chr22: 37,878,171-37,888,423 , GRCh37.p13 chr22: 38,274,178-38,284,430 EIF3L
    nsv7034568copy number variation1nstd229human GRCh38 chr22: 37,846,717-37,848,871 , GRCh37.p13 chr22: 38,242,724-38,244,878 MIR659, ANKRD54, 1 more genes
    nsv7031076copy number variation1nstd229human GRCh38 chr22: 37,878,401-37,883,900 , GRCh37.p13 chr22: 38,274,408-38,279,907 EIF3L
    nsv7029138copy number variation1nstd229human GRCh38 chr22: 37,851,247-37,851,443 , GRCh37.p13 chr22: 38,247,254-38,247,450 EIF3L
    nsv7024528copy number variation1nstd229human GRCh38 chr22: 37,876,012-37,877,673 , GRCh37.p13 chr22: 38,272,019-38,273,680 EIF3L
    nsv7018463copy number variation1nstd229human GRCh38 chr22: 37,845,511-37,847,758 , GRCh37.p13 chr22: 38,241,518-38,243,765 ANKRD54, MIR659, 1 more genes
    nsv7018245copy number variation1nstd229human GRCh38 chr22: 37,884,270-37,895,373 , GRCh37.p13 chr22: 38,280,277-38,291,380 RNU6-900P, EIF3L
    nsv6598454inversion1nstd223human GRCh38 chr22: 37,879,088-37,879,494 , GRCh37.p13 chr22: 38,275,095-38,275,501 EIF3L
    nsv6598281inversion1nstd223human GRCh38 chr22: 37,867,691-37,868,139 , GRCh37.p13 chr22: 38,263,698-38,264,146 EIF3L
    nsv6313943copy number variation1nstd102humanLikely pathogenic GRCh37 chr22: 38,116,341-38,369,048 , GRCh38.p12 chr22: 37,720,334-37,973,041 H1-0, POLR2F, 13 more genes
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