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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7054247inversion1nstd229human GRCh38 chr6: 18,141,080-21,441,150 , GRCh37.p13 chr6: 18,141,311-21,441,381 TPMT, LOC105374965, 37 more genes
    nsv7046409inversion1nstd229human GRCh38 chr6: 18,441,635-18,442,681 , GRCh37.p13 chr6: 18,441,866-18,442,912 RNF144B
    nsv6795733copy number variation1nstd229human GRCh38 chr6: 18,365,101-18,394,600 , GRCh37.p13 chr6: 18,365,332-18,394,831 IMPDH1P9, RNF144B, 1 more genes
    nsv6793580copy number variation1nstd229human GRCh38 chr6: 18,401,859-18,402,640 , GRCh37.p13 chr6: 18,402,090-18,402,871 RNF144B
    nsv6791245copy number variation1nstd229human GRCh38 chr6: 18,465,200-18,468,894 , GRCh37.p13 chr6: 18,465,431-18,469,125 RNF144B
    nsv6790846copy number variation1nstd229human GRCh38 chr6: 18,432,528-18,438,388 , GRCh37.p13 chr6: 18,432,759-18,438,619 RNF144B
    nsv6790565copy number variation1nstd229human GRCh38 chr6: 16,741,614-19,141,206 , GRCh37.p13 chr6: 16,741,845-19,141,437 LOC105374951, RNU6-263P, 34 more genes
    nsv6788565copy number variation1nstd229human GRCh38 chr6: 18,406,701-18,409,000 , GRCh37.p13 chr6: 18,406,932-18,409,231 RNF144B
    nsv6787943copy number variation1nstd229human GRCh38 chr6: 18,399,101-18,403,400 , GRCh37.p13 chr6: 18,399,332-18,403,631 RNF144B
    nsv6787161copy number variation1nstd229human GRCh38 chr6: 17,996,181-18,488,731 , GRCh37.p13 chr6: 17,996,412-18,488,962 NHLRC1, TPMT, 6 more genes
    nsv6782995copy number variation1nstd229human GRCh38 chr6: 18,466,302-18,466,375 , GRCh37.p13 chr6: 18,466,533-18,466,606 RNF144B
    nsv6780784copy number variation1nstd229human GRCh38 chr6: 18,381,141-18,386,218 , GRCh37.p13 chr6: 18,381,372-18,386,449 RNF144B
    nsv6780077copy number variation1nstd229human GRCh38 chr6: 18,455,219-18,473,357 , GRCh37.p13 chr6: 18,455,450-18,473,588 RNF144B
    nsv6778725copy number variation1nstd229human GRCh38 chr6: 18,440,801-18,461,100 , GRCh37.p13 chr6: 18,441,032-18,461,331 RNF144B
    nsv6778137copy number variation1nstd229human GRCh38 chr6: 18,432,558-18,454,368 , GRCh37.p13 chr6: 18,432,789-18,454,599 RNF144B
    nsv6636333copy number variation1nstd102humanPathogenic GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418 SOX4, MDH1P2, 136 more genes
    nsv6567594inversion1nstd223human GRCh38 chr6: 18,409,376-18,409,624 , GRCh37.p13 chr6: 18,409,607-18,409,855 RNF144B
    nsv6411286copy number variation1nstd223human GRCh38 chr6: 18,401,859-18,402,636 , GRCh37.p13 chr6: 18,402,090-18,402,867 RNF144B
    nsv6408118copy number variation1nstd223human GRCh38 chr6: 18,409,586-18,411,518 , GRCh37.p13 chr6: 18,409,817-18,411,749 RNF144B
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