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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143505copy number variation1nstd232human GRCh37.p13 chr19: 40,883,791-40,883,890 , GRCh38.p12 chr19: 40,377,884-40,377,983 PLD3, HIPK4
    nsv7095480copy number variation4nstd102humanUncertain significance GRCh37 chr19: 39,904,727-42,931,301 , GRCh38.p12 chr19: 39,414,087-42,427,149 CYP2B6, EID2B, 140 more genes
    nsv7095278copy number variation1nstd102humanUncertain significance GRCh37 chr19: 40,882,496-41,135,455 , GRCh38.p12 chr19: 40,376,589-40,629,550 HIPK4, PRX, 8 more genes
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 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
    nsv7016371copy number variation1nstd229human GRCh38 chr19: 40,338,494-40,399,272 , GRCh37.p13 chr19: 40,844,401-40,905,179 HIPK4, C19orf47, 3 more genes
    nsv7010304copy number variation1nstd229human GRCh38 chr19: 40,378,976-40,379,118 , GRCh37.p13 chr19: 40,884,883-40,885,025 PLD3, HIPK4
    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
    nsv7006052copy number variation1nstd229human GRCh38 chr19: 40,381,999-40,405,425 , GRCh37.p13 chr19: 40,887,906-40,911,332 HIPK4, PRX
    nsv7002183copy number variation1nstd229human GRCh38 chr19: 40,225,202-40,756,025 , GRCh37.p13 chr19: 40,731,109-41,261,930 RNU6-195P, LTBP4, 21 more genes
    nsv6624898copy number variation1nstd224human GRCh37 chr19: 40,816,530-40,901,531 , GRCh38.p12 chr19: 40,310,623-40,395,624 C19orf47, HIPK4, 3 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6531478copy number variation1nstd223human GRCh38 chr19: 40,386,165-40,387,574 , GRCh37.p13 chr19: 40,892,072-40,893,481 HIPK4
    nsv6524929copy number variation1nstd223human GRCh38 chr19: 40,381,811-40,383,083 , GRCh37.p13 chr19: 40,887,718-40,888,990 HIPK4
    nsv6517572copy number variation1nstd223human GRCh38 chr19: 40,388,998-40,391,380 , GRCh37.p13 chr19: 40,894,905-40,897,287 HIPK4
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6224278copy number variation1nstd214human GRCh38 chr19: 40,377,282-40,377,349 , GRCh37.p13 chr19: 40,883,189-40,883,256 HIPK4, PLD3
    nsv6219669copy number variation1nstd214human GRCh38 chr19: 40,377,059-40,377,296 , GRCh37.p13 chr19: 40,882,966-40,883,203 PLD3, HIPK4
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