ClinVar Miner

List of variants in gene combination ALDOA, ASPHD1, BOLA2, C16orf54, C16orf92, CDIPT, CORO1A, DOC2A, GDPD3, HIRIP3, INO80E, KCTD13, KIF22, MAPK3, MAZ, MVP, PAGR1, PPP4C, PRRT2, QPRT, SEZ6L2, SLX1B, SPN, SULT1A4, TAOK2, TBX6, TLCD3B, TMEM219, YPEL3, ZG16 reported as pathogenic for 16p11.2 deletion syndrome

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Total variants: 1
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GRCh37/hg19 16p11.2(chr16:29042050-30199025)

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