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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6596271inversion1nstd223human GRCh38 chr19: 42,518,252-42,518,613 , GRCh37.p13 chr19: 43,022,404-43,022,765 CEACAM1, LIPE-AS1
    nsv6595594inversion1nstd223human GRCh38 chr19: 41,797,668-42,527,301 , GRCh37.p13 chr19: 42,514,712-43,031,453 GRIK5, CEACAM1, 34 more genes
    nsv6530727copy number variation1nstd223human GRCh38 chr19: 42,507,761-42,510,937 , GRCh37.p13 chr19: 43,011,913-43,015,089 LIPE-AS1, CEACAM1
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv5562413sequence alteration1nstd206human GRCh38 chr19: 41,797,706-42,527,281 , GRCh37.p13 chr19: 42,514,712-43,031,433 MEGF8, LIPE, 34 more genes
    nsv5359813translocation1nstd200human GRCh38 chr19: 42,525,385-42,525,385 , GRCh38 chr19: 42,525,452-42,525,452 , GRCh37.p13 chr19: 43,029,537-43,029,537 , GRCh37.p13 chr19: 43,029,604-43,029,604 CEACAM1, LIPE-AS1, 1 more genes
    nsv5020535copy number variation1nstd200human GRCh38 chr19: 42,493,586-42,679,716 , GRCh37.p13 chr19: 42,997,738-43,183,868 CEACAM1, CEACAMP5, 6 more genes
    nsv4715396copy number variation1nstd195human GRCh38.p12 chr19: 42,419,999-42,609,899 , GRCh37 chr19: 42,924,151-43,114,051 CEACAM1, CEACAM8, 7 more genes
    nsv4534722copy number variation1nstd166human GRCh37.p13 chr19: 42,930,999-43,263,000 , GRCh38.p12 chr19: 42,426,847-42,758,848 LIPE, CXCL17, 12 more genes
    nsv4513282mobile element insertion1nstd166human GRCh37.p13 chr19: 43,020,567-43,020,567 , GRCh38.p12 chr19: 42,516,415-42,516,415 CEACAM1, LIPE-AS1
    nsv4500379mobile element insertion1nstd166human GRCh37.p13 chr19: 43,028,108-43,028,108 , GRCh38.p12 chr19: 42,523,956-42,523,956 CEACAM1, LIPE-AS1, 1 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
    nsv4259973copy number variation1nstd166human GRCh37.p13 chr19: 42,937,017-43,829,931 , GRCh38.p12 chr19: 42,432,865-43,325,779 , CEACAM8, 31 more genes
    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
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