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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5562413sequence alteration1nstd206human GRCh38 chr19: 41,797,706-42,527,281 , GRCh37.p13 chr19: 42,514,712-43,031,433 MEGF8, LIPE, 34 more genes
    nsv5554149sequence alteration1nstd206human GRCh38 chr19: 41,749,279-42,444,786 , GRCh37.p13 chr19: 42,514,712-42,948,938 ERF, CEACAM6, 32 more genes
    nsv5523465copy number variation1nstd206human GRCh38 chr19: 42,314,080-42,314,179 , GRCh37.p13 chr19: 42,818,232-42,818,331 TMEM145
    nsv5516359copy number variation1nstd206human GRCh38 chr19: 42,319,485-42,319,798 , GRCh37.p13 chr19: 42,823,637-42,823,950 TMEM145
    nsv5024664copy number variation1nstd200human GRCh38 chr19: 42,322,727-42,332,554 , GRCh37.p13 chr19: 42,826,879-42,836,706 TMEM145, MEGF8
    nsv4575046mobile element insertion1nstd166human GRCh37.p13 chr19: 42,816,570-42,816,570 , GRCh38.p12 chr19: 42,312,418-42,312,418 TMEM145
    nsv4535045copy number variation1nstd166human GRCh37.p13 chr19: 42,786,999-42,889,000 , GRCh38.p12 chr19: 42,282,847-42,384,848 MEGF8, PAFAH1B3, 4 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4268883copy number variation1nstd166human GRCh37.p13 chr19: 42,818,232-42,818,331 , GRCh38.p12 chr19: 42,314,080-42,314,179 TMEM145
    nsv3921916copy number variation1nstd102humanPathogenic NCBI36 chr19: 47,126,886-48,337,448 , GRCh37 chr19: 42,514,712-43,645,608 , GRCh38 chr19: 41,930,894-43,141,456 PSG6, RABAC1, 42 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3880735copy number variation1nstd102humanLikely pathogenic GRCh38 chr19: 41,608,672-44,315,856 , GRCh37.p13 chr19: 42,514,712-44,820,009 ATP1A3, CEACAM1, 114 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3164963copy number variation1nstd151human GRCh37 chr19: 42,819,521-42,820,897 , GRCh38.p12 chr19: 42,315,369-42,316,745 TMEM145
    nsv3164120copy number variation1nstd151human GRCh37 chr19: 42,798,725-42,946,989 , GRCh38.p12 chr19: 42,294,573-42,442,837 MIR8077, MEGF8, 9 more genes
    nsv3160142copy number variation2nstd151human GRCh37 chr19: 42,813,734-42,820,897 , GRCh38.p12 chr19: 42,309,582-42,316,745 TMEM145, PRR19
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