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Items: 1 to 20 of 260

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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
    nsv7039501inversion1nstd229human GRCh38 chr5: 149,317,633-149,317,752 , GRCh37.p13 chr5: 148,697,196-148,697,315 AFAP1L1
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6796209copy number variation1nstd229human GRCh38 chr5: 149,254,956-149,344,332 , GRCh37.p13 chr5: 148,634,519-148,723,895 AFAP1L1, ABLIM3, 1 more genes
    nsv6795983copy number variation1nstd229human GRCh38 chr5: 149,268,821-149,271,325 , GRCh37.p13 chr5: 148,648,384-148,650,888 AFAP1L1
    nsv6795917copy number variation1nstd229human GRCh38 chr5: 149,307,540-149,312,472 , GRCh37.p13 chr5: 148,687,103-148,692,035 AFAP1L1
    nsv6791998copy number variation1nstd229human GRCh38 chr5: 149,327,063-149,327,300 , GRCh37.p13 chr5: 148,706,626-148,706,863 AFAP1L1
    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
    nsv6405777copy number variation1nstd223human GRCh38 chr5: 149,302,970-149,309,698 , GRCh37.p13 chr5: 148,682,533-148,689,261 AFAP1L1
    nsv6294075mobile element insertion1nstd186human GRCh37 chr5: 148,661,284-148,661,335 , GRCh38.p12 chr5: 149,281,721-149,281,772 AFAP1L1
    nsv6280069insertion1nstd214human GRCh38 chr5: 149,327,063-149,327,063 , GRCh37.p13 chr5: 148,706,626-148,706,626 AFAP1L1
    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
    nsv6020279copy number variation1nstd212human GRCh38 chr5: 149,274,610-149,274,686 , GRCh37.p13 chr5: 148,654,173-148,654,249 AFAP1L1
    nsv6019576copy number variation1nstd212human GRCh38 chr5: 149,327,060-149,327,300 , GRCh37.p13 chr5: 148,706,623-148,706,863 AFAP1L1
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