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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7041752inversion1nstd229human GRCh38 chr5: 149,368,601-149,368,614 , GRCh37.p13 chr5: 148,748,164-148,748,177 PCYOX1L
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6791161copy number variation1nstd229human GRCh38 chr5: 149,347,479-149,356,494 , GRCh37.p13 chr5: 148,727,042-148,736,057 PCYOX1L, GRPEL2-AS1, 1 more genes
    nsv6787016copy number variation1nstd229human GRCh38 chr5: 149,369,532-149,375,453 , GRCh37.p13 chr5: 148,749,095-148,755,016 IL17B, PCYOX1L
    nsv6778492copy number variation1nstd229human GRCh38 chr5: 149,324,099-149,359,426 , GRCh37.p13 chr5: 148,703,662-148,738,989 PCYOX1L, AFAP1L1, 2 more genes
    nsv6636986copy number variation1nstd102humanPathogenic GRCh37 chr5: 147,164,969-149,315,489 , GRCh38.p12 chr5: 147,785,406-149,935,926 GRPEL2-AS1, PDE6A, 43 more genes
    nsv6400286copy number variation1nstd223human GRCh38 chr5: 149,369,532-149,375,449 , GRCh37.p13 chr5: 148,749,095-148,755,012 IL17B, PCYOX1L
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135120copy number variation1nstd213human GRCh37 chr5: 143,910,000-152,670,001 , GRCh38.p12 chr5: 144,530,437-153,290,441 ADRB2, ANXA6, 143 more genes
    nsv6134980copy number variation1nstd213human GRCh37 chr5: 147,840,000-149,100,001 , GRCh38.p12 chr5: 148,460,437-149,720,438 ABLIM3, SH3TC2, 22 more genes
    nsv6069916insertion1nstd212human GRCh38 chr5: 149,370,031-149,370,031 , GRCh37.p13 chr5: 148,749,594-148,749,594 PCYOX1L
    nsv5950999insertion1nstd209human GRCh38 chr5: 149,370,028-149,370,028 , GRCh37.p13 chr5: 148,749,591-148,749,591 PCYOX1L
    nsv5634188insertion1nstd207human GRCh38 chr5: 149,370,033-149,370,033 , GRCh37.p13 chr5: 148,749,596-148,749,596 PCYOX1L
    nsv5552999insertion1nstd206human GRCh38 chr5: 149,370,028-149,370,061 , GRCh37.p13 chr5: 148,749,591-148,749,624 PCYOX1L
    nsv5097677mobile element insertion1nstd203human GRCh38 chr5: 149,370,024-149,370,061 , GRCh37.p13 chr5: 148,749,587-148,749,624 PCYOX1L
    nsv5097029mobile element insertion1nstd203human GRCh38 chr5: 149,370,019-149,370,067 , GRCh37.p13 chr5: 148,749,582-148,749,630 PCYOX1L
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