HIFTD: Human infertility and fetal tissue database


Human infertility and fetal tissue database mainly contains the genomic sequencing information of several diseases which relate to human reproductive function, including infertility, recurrent miscarriage, azoospermia, polycystic ovary syndrome, uterine fibroid, endometriosis, adenomyosis etc. In addition, the database also includes sequencing data of fetal tissue and normal individuals. Human infertility and fetal tissue database provide SNPs (single nucleotide polymorphisms), InDels (small Insertions and Deletions, shorter than 50bp), CNVs (copy number variants: including deletions and insertions) and SVs (structural variants: including translocations and inversions) for clinicians and researchers.

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Note: Only provide public data search results. you can enter project name, gene , sample code , rsID , transcript(NM_XXXX) , or variation as keyword. variation examples: chr1:1234, chr1:1234:A:G, chr1:196777254-196918801

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