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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137731copy number variation1nstd102humanBenign GRCh37 chrX: 1,412,907-1,412,990 , GRCh38 chrX: 1,294,014-1,294,097 , GRCh38 chrY: 1,294,014-1,294,097 , GRCh37 chrY: 1,362,907-1,362,990 CSF2RA, MIR3690
    nsv6128074insertion1nstd186human GRCh37 chrX: 1,389,811-1,389,811 , GRCh38.p12 chrX: 1,270,918-1,270,918 CSF2RA
    nsv6127613insertion1nstd186human GRCh37 chrX: 1,413,967-1,413,967 , GRCh38.p12 chrX: 1,295,074-1,295,074 CSF2RA
    nsv6125241insertion1nstd186human GRCh37 chrX: 1,393,469-1,393,469 , GRCh38.p12 chrX: 1,274,576-1,274,576 CSF2RA
    nsv6116896copy number variation1nstd186human GRCh37 chrX: 1,433,437-1,433,744 , GRCh38.p12 chrX: 1,314,544-1,314,851 CSF2RA
    nsv6116618copy number variation1nstd186human GRCh37 chrX: 1,403,325-1,403,575 , GRCh38.p12 chrX: 1,284,432-1,284,682 CSF2RA
    nsv6116355copy number variation1nstd186human GRCh37 chrX: 1,406,545-1,406,839 , GRCh38.p12 chrX: 1,287,652-1,287,946 CSF2RA
    nsv6113218copy number variation1nstd186human GRCh37 chrX: 1,390,102-1,390,250 , GRCh38.p12 chrX: 1,271,209-1,271,357 CSF2RA
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5980182copy number variation1nstd209human GRCh38 chrX: 1,298,243-1,300,973 , GRCh37.p13 chrX: 1,417,136-1,419,866 CSF2RA, RNA5SP498
    nsv5979445inversion1nstd209human GRCh37.p13 chrX: 1,407,329-1,411,037 , GRCh38 chrX: 1,288,436-1,292,144 , CSF2RA, 1 more genes
    nsv5979057copy number variation1nstd209human GRCh38 chrX: 1,293,958-1,296,373 , GRCh37.p13 chrX: 1,412,851-1,415,266 CSF2RA, MIR3690
    nsv5976632copy number variation1nstd209human GRCh38 chrX: 1,264,675-1,277,309 , GRCh37.p13 chrX: 1,383,568-1,396,202 CSF2RA
    nsv5976424copy number variation1nstd209human GRCh38 chrX: 1,260,730-1,267,140 , GRCh37.p13 chrX: 1,379,623-1,386,033 , CSF2RA
    nsv5976269copy number variation1nstd209human GRCh38 chrX: 1,304,843-1,319,357 , GRCh37.p13 chrX: 1,423,736-1,438,250 CSF2RA
    nsv5975651copy number variation3nstd209human GRCh38 chrX: 1,323,318-1,327,260 , GRCh37.p13 chrX: 1,442,211-1,446,153 CSF2RA
    nsv5975389copy number variation2nstd209human GRCh38 chrX: 1,320,758-1,326,560 , GRCh37.p13 chrX: 1,439,651-1,445,453 CSF2RA
    nsv5974826copy number variation2nstd209human GRCh38 chrX: 1,304,693-1,307,312 , GRCh37.p13 chrX: 1,423,586-1,426,205 CSF2RA
    nsv5973939copy number variation1nstd209human GRCh38 chrX: 1,301,474-1,303,981 , GRCh37.p13 chrX: 1,420,367-1,422,874 CSF2RA
    nsv5973413copy number variation2nstd209human GRCh38 chrX: 1,291,126-1,293,657 , GRCh37.p13 chrX: 1,410,019-1,412,550 , CSF2RA, 1 more genes
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