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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv7017979copy number variation1nstd229human GRCh38 chr19: 39,527,600-39,533,921 , GRCh37.p13 chr19: 40,018,240-40,024,561 CRIPTOP7, EID2B
    nsv7008627copy number variation1nstd229human GRCh38 chr19: 39,364,901-39,554,300 , GRCh37.p13 chr19: 39,855,541-40,044,940 CRIPTOP7, ZFP36, 16 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
    nsv7007120copy number variation1nstd229human GRCh38 chr19: 39,511,623-39,657,771 , GRCh37.p13 chr19: 40,002,263-40,148,411 LGALS13, LGALS16, 10 more genes
    nsv7006517copy number variation1nstd229human GRCh38 chr19: 39,517,058-39,536,626 , GRCh37.p13 chr19: 40,007,698-40,027,266 SELENOV, EID2B, 1 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7005664copy number variation1nstd229human GRCh38 chr19: 39,530,314-39,535,339 , GRCh37.p13 chr19: 40,020,954-40,025,979 CRIPTOP7, EID2B
    nsv6595672inversion1nstd223human GRCh38 chr19: 39,529,286-39,529,998 , GRCh37.p13 chr19: 40,019,926-40,020,638 EID2B
    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
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5710918mobile element insertion1nstd211human GRCh38 chr19: 39,530,679-39,530,679 , GRCh37.p13 chr19: 40,021,319-40,021,319 EID2B
    nsv5531093copy number variation1nstd206human GRCh38 chr19: 39,530,314-39,535,333 , GRCh37.p13 chr19: 40,020,954-40,025,973 EID2B, CRIPTOP7
    nsv5282884copy number variation1nstd204human GRCh38.p13 chr19: 39,528,140-39,529,192 , GRCh37.p13 chr19: 40,018,780-40,019,832 EID2B
    nsv4707508copy number variation1nstd195human GRCh38.p12 chr19: 39,530,511-39,628,061 , GRCh37 chr19: 40,021,151-40,118,701 LGALS13, EID2B, 6 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
    nsv4413993copy number variation1nstd174human GRCh37 chr19: 40,019,489-40,027,856 , GRCh38.p12 chr19: 39,528,849-39,537,216 CRIPTOP7, EID2, 1 more genes
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