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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130992insertion1nstd186human GRCh37 chr19: 21,131,388-21,565,847 , GRCh38.p12 chr19: 20,948,582-21,383,045 RPL36AP51, LOC107985265, 16 more genes
    nsv5977389inversion1nstd209human GRCh38 chr19: 20,812,138-20,994,800 , GRCh37.p13 chr19: 20,994,944-21,177,606 ZNF85, KRT18P40, 9 more genes
    nsv5977341inversion1nstd209human GRCh38 chr19: 20,769,287-20,965,951 , GRCh37.p13 chr19: 20,952,093-21,148,757 ZNF66, ZNF85, 10 more genes
    nsv5970427inversion1nstd209human GRCh38 chr19: 20,770,935-20,970,953 , GRCh37.p13 chr19: 20,953,741-21,153,759 ZNF66, ZNF85, 11 more genes
    nsv5939330copy number variation1nstd209human GRCh38 chr19: 20,960,491-20,960,554 , GRCh37.p13 chr19: 21,143,297-21,143,360 KRT18P40
    nsv5872743copy number variation1nstd209human GRCh38 chr19: 20,949,849-20,976,116 , GRCh37.p13 chr19: 21,132,655-21,158,922 KRT18P40, LOC112268247, 1 more genes
    nsv5540404insertion1nstd206human GRCh38 chr19: 20,948,582-21,383,045 , GRCh37.p13 chr19: 21,131,388-21,565,847 RPL7AP10, VN1R81P, 16 more genes
    nsv5520281copy number variation1nstd206human GRCh38 chr19: 20,960,493-20,960,555 , GRCh37.p13 chr19: 21,143,299-21,143,361 KRT18P40
    nsv5359591translocation1nstd200human GRCh38 chr19: 20,960,555-20,960,555 , GRCh38 chr19: 20,960,493-20,960,493 , GRCh37.p13 chr19: 21,143,299-21,143,299 , GRCh37.p13 chr19: 21,143,361-21,143,361 KRT18P40
    nsv5338967translocation1nstd200human GRCh37 chr19: 21,143,361-21,143,361 , GRCh37 chr19: 21,143,299-21,143,299 , GRCh38.p12 chr19: 20,960,493-20,960,493 , GRCh38.p12 chr19: 20,960,555-20,960,555 , GRCh38.p12 chr19|NW_003315962.1: 303,831-303,831 , GRCh38.p12 chr19|NW_003315962.1: 303,769-303,769 KRT18P40
    nsv5019533copy number variation1nstd200human GRCh38 chr19: 20,181,329-20,983,243 , GRCh37.p13 chr19: 20,292,138-20,845,948 , GRCh37.p13 chr19|NW_003571053.2: 98,582-580,395 , MIR1270, 37 more genes
    nsv5014719copy number variation1nstd200human GRCh38 chr19: 20,909,191-20,961,132 , GRCh37.p13 chr19: 21,091,997-21,143,938 LOC100418992, LOC100418993, 2 more genes
    nsv4436023complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 19,120,059-23,932,567 , GRCh37 chr19: 19,230,868-24,115,369 NCAN, BORCS8-MEF2B, 195 more genes
    nsv4420095copy number variation1nstd174human GRCh37 chr19: 21,000,562-21,177,577 , GRCh38.p12 chr19: 20,817,756-20,994,771 , GRCh38.p12 chr19|NW_003315962.1: 154,741-338,047 LOC100418986, LOC100418989, 9 more genes
    nsv4255887copy number variation1nstd166human GRCh37.p13 chr19: 21,143,299-21,143,361 , GRCh38.p12 chr19: 20,960,493-20,960,555 , GRCh38.p12 chr19|NW_003315962.1: 303,769-303,831 KRT18P40
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 more genes
    nsv3921076copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,133,594-24,193,591 , GRCh37 chr19: 15,244,405-24,376,393 , NCBI36 chr19: 15,105,405-24,168,233 MRPL34, BNIP3P25, 358 more genes
    nsv3920966copy number variation1nstd102humanUncertain significance GRCh38 chr19: 20,859,049-21,165,434 , GRCh37 chr19: 21,041,855-21,348,237 , NCBI36 chr19: 20,833,695-21,140,077 LOC100418990, VN1R80P, 16 more genes
    nsv3918940copy number variation1nstd102humanUncertain significance GRCh37 chr19: 20,820,793-22,159,018 , GRCh38 chr19: 20,637,987-21,976,216 , NCBI36 chr19: 20,612,633-21,950,858 LOC100418988, LOC100418991, 51 more genes
    nsv3915707copy number variation1nstd102humanUncertain significance NCBI36 chr19: 19,739,311-21,068,211 , GRCh38 chr19: 19,767,502-21,093,565 , GRCh37 chr19: 19,878,311-21,276,371 KRT18P40, BNIP3P22, 60 more genes
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