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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6621798copy number variation1nstd224human GRCh37 chr12: 37,960,135-38,443,752 , GRCh38.p12 chr12: 37,566,333-38,049,950 ZNF970P
    nsv6621797copy number variation1nstd224human GRCh37 chr12: 37,960,135-38,314,305 , GRCh38.p12 chr12: 37,566,333-37,920,503 ZNF970P
    nsv6621796copy number variation2nstd224human GRCh37 chr12: 37,927,114-38,361,657 , GRCh38.p12 chr12: 37,533,312-37,967,855 ZNF970P
    nsv6621698copy number variation1nstd224human GRCh37 chr12: 37,960,135-38,120,936 , GRCh38.p12 chr12: 37,566,333-37,727,134 ZNF970P
    nsv6621615copy number variation1nstd224human GRCh37 chr12: 37,961,768-38,475,465 , GRCh38.p12 chr12: 37,567,966-38,081,663 CLUHP8, ZNF970P, 1 more genes
    nsv6621614copy number variation1nstd224human GRCh37 chr12: 37,891,419-38,086,915 , GRCh38.p12 chr12: 37,497,617-37,693,113 ZNF970P
    nsv6621466copy number variation1nstd224human GRCh37 chr12: 37,927,114-38,166,006 , GRCh38.p12 chr12: 37,533,312-37,772,204 ZNF970P
    nsv6621465copy number variation2nstd224human GRCh37 chr12: 37,927,114-37,995,364 , GRCh38.p12 chr12: 37,533,312-37,601,562 ZNF970P
    nsv6621464copy number variation1nstd224human GRCh37 chr12: 37,891,419-38,228,251 , GRCh38.p12 chr12: 37,497,617-37,834,449 ZNF970P
    nsv6621350copy number variation1nstd224human GRCh37 chr12: 37,960,135-38,623,564 , GRCh38.p12 chr12: 37,566,333-38,229,762 TUBB8P5, AK6P2, 7 more genes
    nsv6621349copy number variation1nstd224human GRCh37 chr12: 37,960,135-38,118,144 , GRCh38.p12 chr12: 37,566,333-37,724,342 ZNF970P
    nsv6132695copy number variation1nstd213human GRCh37 chr12: 37,860,000-42,780,001 , GRCh38.p12 chr12: 37,466,198-42,386,199 PDZRN4, SLC2A13, 48 more genes
    nsv5926733copy number variation1nstd209human GRCh38 chr12: 34,019,538-38,313,749 , GRCh37.p13 chr12: 34,172,473-38,707,551 AK6P1, AK6P2, 12 more genes
    nsv5926102copy number variation1nstd209human GRCh38 chr12: 37,411,012-38,025,679 , GRCh37.p13 chr12: 37,856,695-38,419,481 ZNF970P
    nsv5924332copy number variation1nstd209human GRCh38 chr12: 37,544,062-37,613,234 , GRCh37.p13 chr12: 37,937,864-38,007,036 ZNF970P
    nsv5910429copy number variation1nstd209human GRCh38 chr12: 34,050,005-38,345,840 , GRCh37.p13 chr12: 34,202,940-38,739,642 LOC107984469, ALG10B, 12 more genes
    nsv5909911copy number variation1nstd209human GRCh38 chr12: 37,577,559-37,577,867 , GRCh37.p13 chr12: 37,971,361-37,971,669 ZNF970P
    nsv5864380copy number variation1nstd209human GRCh38 chr12: 37,565,294-37,585,599 , GRCh37.p13 chr12: 37,959,096-37,979,401 ZNF970P
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
    nsv4985293copy number variation1nstd200human GRCh38 chr12: 37,517,549-37,751,948 , GRCh37.p13 chr12: 37,911,351-38,145,750 ZNF970P
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