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Items: 1 to 20 of 389

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143902copy number variation1nstd232human GRCh37.p13 chr5: 149,148,165-149,148,236 , GRCh38.p12 chr5: 149,768,602-149,768,673 PPARGC1B
    nsv7097513copy number variation1nstd102humanUncertain significance GRCh37 chr5: 147,774,340-149,681,936 , GRCh38.p12 chr5: 148,394,777-150,302,373 CSNK1A1, SLC26A2, 39 more genes
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7053584inversion1nstd229human GRCh38 chr5: 144,534,922-150,861,041 , GRCh37.p13 chr5: 143,914,485-150,240,603 SMIM3, NAMPTP2, 102 more genes
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6797282copy number variation1nstd229human GRCh38 chr5: 149,794,733-149,797,507 , GRCh37.p13 chr5: 149,174,296-149,177,070 PPARGC1B
    nsv6795881copy number variation1nstd229human GRCh38 chr5: 149,768,032-149,775,077 , GRCh37.p13 chr5: 149,147,595-149,154,640 PPARGC1B
    nsv6795714copy number variation1nstd229human GRCh38 chr5: 149,770,497-149,773,978 , GRCh37.p13 chr5: 149,150,060-149,153,541 PPARGC1B
    nsv6793303copy number variation1nstd229human GRCh38 chr5: 149,809,903-149,810,661 , GRCh37.p13 chr5: 149,189,466-149,190,224 PPARGC1B
    nsv6792624copy number variation1nstd229human GRCh38 chr5: 149,737,279-149,740,951 , GRCh37.p13 chr5: 149,116,842-149,120,514 PPARGC1B
    nsv6792327copy number variation1nstd229human GRCh38 chr5: 149,845,291-149,845,665 , GRCh37.p13 chr5: 149,224,854-149,225,228 PPARGC1B
    nsv6791840copy number variation1nstd229human GRCh38 chr5: 149,763,970-149,768,186 , GRCh37.p13 chr5: 149,143,533-149,147,749 PPARGC1B
    nsv6788591copy number variation1nstd229human GRCh38 chr5: 149,805,374-149,811,912 , GRCh37.p13 chr5: 149,184,937-149,191,475 PPARGC1B
    nsv6787637copy number variation1nstd229human GRCh38 chr5: 149,740,304-149,740,517 , GRCh37.p13 chr5: 149,119,867-149,120,080 PPARGC1B
    nsv6787214copy number variation1nstd229human GRCh38 chr5: 149,768,602-149,768,674 , GRCh37.p13 chr5: 149,148,165-149,148,237 PPARGC1B
    nsv6787102copy number variation1nstd229human GRCh38 chr5: 149,792,001-149,794,688 , GRCh37.p13 chr5: 149,171,564-149,174,251 PPARGC1B
    nsv6785376copy number variation1nstd229human GRCh38 chr5: 149,850,618-149,890,636 , GRCh37.p13 chr5: 149,230,181-149,270,199 PPARGC1B, PDE6A
    nsv6783737copy number variation1nstd229human GRCh38 chr5: 149,816,201-149,820,500 , GRCh37.p13 chr5: 149,195,764-149,200,063 PPARGC1B
    nsv6781880copy number variation1nstd229human GRCh38 chr5: 149,709,401-149,948,000 , GRCh37.p13 chr5: 149,088,964-149,327,563 PDE6A, MIR378A, 4 more genes
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