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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097240copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,616,098-159,618,829 , GRCh38.p12 chr4: 158,694,946-158,697,677 ETFDH
    nsv7096839copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,606,119-159,616,730 , GRCh38.p12 chr4: 158,684,967-158,695,578 ETFDH
    nsv7096838copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,593,534-159,629,689 , GRCh38.p12 chr4: 158,672,382-158,708,537 PPID, C4orf46, 1 more genes
    nsv7054636inversion1nstd229human GRCh38 chr4: 158,671,571-158,703,220 , GRCh37.p13 chr4: 159,592,723-159,624,372 C4orf46, ETFDH
    nsv7050285inversion1nstd229human GRCh38 chr4: 158,699,001-158,706,358 , GRCh37.p13 chr4: 159,620,153-159,627,510 ETFDH
    nsv7046716inversion1nstd229human GRCh38 chr4: 158,656,634-158,673,753 , GRCh37.p13 chr4: 159,577,786-159,594,905 C4orf46, ETFDH
    nsv7039335inversion1nstd229human GRCh38 chr4: 158,656,635-158,673,754 , GRCh37.p13 chr4: 159,577,787-159,594,906 ETFDH, C4orf46
    nsv6755470copy number variation1nstd229human GRCh38 chr4: 158,657,968-158,695,768 , GRCh37.p13 chr4: 159,579,120-159,616,920 ETFDH, C4orf46
    nsv6751488copy number variation1nstd229human GRCh38 chr4: 158,656,601-158,703,200 , GRCh37.p13 chr4: 159,577,753-159,624,352 ETFDH, C4orf46
    nsv6750974copy number variation1nstd229human GRCh38 chr4: 158,707,596-158,707,679 , GRCh37.p13 chr4: 159,628,748-159,628,831 PPID, ETFDH
    nsv6743268copy number variation1nstd229human GRCh38 chr4: 158,682,101-158,893,300 , GRCh37.p13 chr4: 159,603,253-159,814,452 PPID, ETFDH, 3 more genes
    nsv6742934copy number variation1nstd229human GRCh38 chr4: 158,677,501-158,734,000 , GRCh37.p13 chr4: 159,598,653-159,655,152 ETFDH, PPID
    nsv6742850copy number variation1nstd229human GRCh38 chr4: 158,640,552-158,728,570 , GRCh37.p13 chr4: 159,561,704-159,649,722 C4orf46, PPID, 2 more genes
    nsv6740281copy number variation1nstd229human GRCh38 chr4: 158,658,715-158,672,239 , GRCh37.p13 chr4: 159,579,867-159,593,391 C4orf46, ETFDH
    nsv6636412copy number variation1nstd102humanUncertain significance GRCh37 chr4: 158,682,606-159,762,612 , GRCh38.p12 chr4: 157,761,454-158,841,460 LOC105377509, GASK1B, 15 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6629567copy number variation1nstd224human GRCh37 chr4: 159,588,973-159,616,703 , GRCh38.p12 chr4: 158,667,821-158,695,551 ETFDH, C4orf46
    nsv6629135copy number variation1nstd224human GRCh37 chr4: 159,601,676-159,620,250 , GRCh38.p12 chr4: 158,680,524-158,699,098 ETFDH
    nsv6565948inversion1nstd223human GRCh38 chr4: 158,691,651-158,692,364 , GRCh37.p13 chr4: 159,612,803-159,613,516 ETFDH
    nsv6565615inversion1nstd223human GRCh38 chr4: 158,500,774-158,878,862 , GRCh37.p13 chr4: 159,421,926-159,800,014 ETFDH, PPID, 4 more genes
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