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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094471copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,322,540-40,326,665 , GRCh38.p12 chr15: 40,030,339-40,034,464 SRP14, EIF2AK4
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6975272copy number variation1nstd229human GRCh38 chr15: 40,029,809-40,030,228 , GRCh37.p13 chr15: 40,322,010-40,322,429 EIF2AK4
    nsv6973253copy number variation1nstd229human GRCh38 chr15: 39,981,444-39,985,740 , GRCh37.p13 chr15: 40,273,645-40,277,941 EIF2AK4
    nsv6968975copy number variation1nstd229human GRCh38 chr15: 39,949,963-39,951,995 , GRCh37.p13 chr15: 40,242,164-40,244,196 H3P38, EIF2AK4
    nsv6964883copy number variation1nstd229human GRCh38 chr15: 39,883,301-41,010,600 , GRCh37.p13 chr15: 40,175,502-41,302,798 SRP14, BUB1B-PAK6, 54 more genes
    nsv6960472copy number variation1nstd229human GRCh38 chr15: 40,022,894-40,024,887 , GRCh37.p13 chr15: 40,315,095-40,317,088 EIF2AK4
    nsv6958691copy number variation1nstd229human GRCh38 chr15: 40,031,688-40,076,143 , GRCh37.p13 chr15: 40,323,889-40,368,344 EIF2AK4, LOC105370787, 2 more genes
    nsv6579625inversion1nstd223human GRCh38 chr15: 40,005,352-40,005,517 , GRCh37.p13 chr15: 40,297,553-40,297,718 EIF2AK4
    nsv6513780copy number variation1nstd223human GRCh38 chr15: 39,915,601-39,938,200 , GRCh37.p13 chr15: 40,207,802-40,230,401 GPR176-DT, GPR176, 1 more genes
    nsv6510537copy number variation1nstd223human GRCh38 chr15: 39,970,701-39,984,700 , GRCh37.p13 chr15: 40,262,902-40,276,901 EIF2AK4
    nsv6509403copy number variation1nstd223human GRCh38 chr15: 39,943,701-39,944,600 , GRCh37.p13 chr15: 40,235,902-40,236,801 EIF2AK4
    nsv6499876copy number variation1nstd223human GRCh38 chr15: 39,961,363-39,961,657 , GRCh37.p13 chr15: 40,253,564-40,253,858 EIF2AK4
    nsv6313915copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,132,892-40,511,958 , GRCh38.p12 chr15: 39,840,691-40,219,757 LOC107984763, BMF, 11 more genes
    nsv6132806copy number variation1nstd213human GRCh37 chr15: 39,170,000-42,090,001 , GRCh38.p12 chr15: 38,877,799-41,797,803 GCHFR, LTK, 84 more genes
    nsv6130535insertion1nstd186human GRCh37 chr15: 40,316,445-40,316,480 , GRCh38.p12 chr15: 40,024,244-40,024,279 EIF2AK4
    nsv6097264insertion1nstd212human GRCh38 chr15: 39,937,287-39,937,287 , GRCh37.p13 chr15: 40,229,488-40,229,488 EIF2AK4
    nsv5939106copy number variation1nstd209human GRCh38 chr15: 38,008,106-40,186,655 , GRCh37.p13 chr15: 38,300,307-40,478,856 , LOC105370784, 36 more genes
    nsv5715157mobile element insertion1nstd211human GRCh38 chr15: 39,949,788-39,949,788 , GRCh37.p13 chr15: 40,241,989-40,241,989 EIF2AK4, H3P38
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