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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139038copy number variation1nstd232human GRCh37.p13 chr19: 5,691,463-5,691,540 , GRCh38.p12 chr19: 5,691,452-5,691,529 LONP1, RPL36
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7069554inversion1nstd229human GRCh38 chr19: 5,658,828-5,764,397 , GRCh37.p13 chr19: 5,658,839-5,764,408 LONP1, MICOS13, 5 more genes
    nsv7068649inversion1nstd229human GRCh38 chr19: 4,313,135-7,007,201 , GRCh37.p13 chr19: 4,313,132-7,007,212 CAPS, SH2D3A, 93 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7066921inversion1nstd229human GRCh38 chr19: 4,809,260-7,077,959 , GRCh37.p13 chr19: 4,809,272-7,077,970 MLLT1, GPR108, 74 more genes
    nsv7063066inversion1nstd229human GRCh38 chr19: 5,490,877-5,786,238 , GRCh37.p13 chr19: 5,490,888-5,786,249 RPL36, CATSPERD, 10 more genes
    nsv7058422inversion1nstd229human GRCh38 chr19: 5,660,768-5,764,254 , GRCh37.p13 chr19: 5,660,779-5,764,265 LONP1, RPL36, 5 more genes
    nsv7016490copy number variation1nstd229human GRCh38 chr19: 5,647,801-5,918,500 , GRCh37.p13 chr19: 5,647,812-5,918,511 CAPS, LONP1, 16 more genes
    nsv7011529copy number variation1nstd229human GRCh38 chr19: 5,502,845-5,861,126 , GRCh37.p13 chr19: 5,502,856-5,861,137 CATSPERD, SAFB, 14 more genes
    nsv7009349copy number variation1nstd229human GRCh38 chr19: 5,661,201-5,741,600 , GRCh37.p13 chr19: 5,661,212-5,741,611 RPL36, LOC107985320, 5 more genes
    nsv7002236copy number variation1nstd229human GRCh38 chr19: 5,692,001-5,695,000 , GRCh37.p13 chr19: 5,692,012-5,695,011 RPL36, LONP1
    nsv7000960copy number variation1nstd229human GRCh38 chr19: 5,692,209-5,693,296 , GRCh37.p13 chr19: 5,692,220-5,693,307 LONP1, RPL36
    nsv6625446copy number variation1nstd224human GRCh37 chr19: 5,649,716-5,756,645 , GRCh38.p12 chr19: 5,649,705-5,756,634 SAFB, LONP1, 5 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6518347copy number variation1nstd223human GRCh38 chr19: 5,519,830-5,914,520 , GRCh37.p13 chr19: 5,519,841-5,914,531 NRTN, VMAC, 19 more genes
    nsv6314807copy number variation1nstd102humanUncertain significance GRCh37 chr19: 5,678,562-5,903,719 , GRCh38.p12 chr19: 5,678,551-5,903,708 VMAC, LOC101928844, 13 more genes
    nsv6310708copy number variation1nstd102humanUncertain significance GRCh37 chr19: 5,678,562-5,897,028 , GRCh38.p12 chr19: 5,678,551-5,897,017 DUS3L, HSD11B1L, 12 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133468copy number variation1nstd213human GRCh37 chr19: 2,040,000-7,300,001 , GRCh38.p12 chr19: 2,040,001-7,299,990 TLE5, AMH, 192 more genes
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