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Items: 1 to 20 of 97

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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
    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
    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
    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
    nsv6566766inversion1nstd223human GRCh38 chr5: 149,348,999-149,350,046 , GRCh37.p13 chr5: 148,728,562-148,729,609 GRPEL2-AS1, GRPEL2
    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
    nsv5456414copy number variation1nstd206human GRCh38 chr5: 149,260,436-149,353,069 , GRCh37.p13 chr5: 148,639,999-148,732,632 ABLIM3, AFAP1L1, 2 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4939138copy number variation1nstd200human GRCh38 chr5: 149,349,043-149,355,105 , GRCh37.p13 chr5: 148,728,606-148,734,668 GRPEL2, GRPEL2-AS1
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4814921copy number variation1nstd200human GRCh37 chr5: 148,728,606-148,734,668 , GRCh38.p12 chr5: 149,349,043-149,355,105 GRPEL2, GRPEL2-AS1
    nsv4457090copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,424,333-148,985,999 , GRCh38.p12 chr5: 141,044,748-149,606,436 PCDHGC4, CKS1BP5, 165 more genes
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