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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5283734copy number variation1nstd204human GRCh38.p13 chr19: 16,184,531-16,192,422 , GRCh37.p13 chr19: 16,295,342-16,303,233 FAM32A
    nsv5183111mobile element insertion1nstd203human GRCh38 chr19: 16,183,560-16,183,571 , GRCh37.p13 chr19: 16,294,371-16,294,382 FAM32A
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4632165copy number variation1nstd183human GRCh37 chr19: 16,164,883-16,303,015 , GRCh38.p12 chr19: 16,054,073-16,192,204 RAB8A, TPM4, 4 more genes
    nsv4573574mobile element insertion1nstd166human GRCh37.p13 chr19: 16,294,371-16,294,371 , GRCh38.p12 chr19: 16,183,560-16,183,560 FAM32A
    nsv4457713copy number variation1nstd102humanUncertain significance GRCh37 chr19: 15,623,742-16,301,544 , GRCh38.p12 chr19: 15,512,931-16,190,733 CIB3, UCA1-AS1, 34 more genes
    nsv4260700copy number variation1nstd166human GRCh37.p13 chr19: 16,288,898-16,295,414 , GRCh38.p12 chr19: 16,178,087-16,184,603 FAM32A
    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
    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
    nsv3909889copy number variation1nstd102humanPathogenic NCBI36 chr19: 14,126,774-16,886,123 , GRCh38 chr19: 14,154,962-16,914,313 , GRCh37 chr19: 14,265,774-17,025,123 OR7A1P, SNRPGP15, 108 more genes
    nsv3908579copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,124,666-16,431,349 , GRCh38.p12 chr19: 14,013,854-16,320,538 TMEM167AP2, TEKTL1, 99 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
    nsv3899292copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,883,158-16,788,770 , GRCh38.p12 chr19: 14,772,346-16,677,959 KLF2, ADGRE2, 80 more genes
    nsv3893972copy number variation1nstd102humanPathogenic GRCh37 chr19: 15,959,347-17,901,296 , GRCh38.p12 chr19: 15,848,537-17,790,487 BABAM1, OR10H4, 70 more genes
    nsv3893745copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 15,921,132-17,479,860 , GRCh38.p12 chr19: 15,810,322-17,369,051 NR2F6, RAB8A, 56 more genes
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