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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5895306copy number variation1nstd209human GRCh38 chr3: 60,551,483-60,743,752 , GRCh37.p13 chr3|NW_003871058.1: 1-171,154 , GRCh37.p13 chr3: 60,558,332-60,729,485 FHIT, TMED2P1, 4 more genes
    nsv5836647copy number variation2nstd209human GRCh38 chr3: 60,731,320-60,732,419 , GRCh37.p13 chr3|NW_003871058.1: 158,722-159,821 , GRCh37.p13 chr3: 60,717,053-60,718,152 PPIAP71, FHIT
    nsv5434955copy number variation1nstd206human GRCh38 chr3: 60,714,000-60,778,000 , GRCh37.p13 chr3|NW_003871058.1: 141,402-205,402 , GRCh37.p13 chr3: 60,699,733-60,763,733 TMED2P1, FHIT, 1 more genes
    nsv5304531copy number variation1nstd204human GRCh38.p13 chr3: 60,346,927-61,679,238 , GRCh37.p13 chr3: 60,332,658-61,664,912 , PTPRG, 9 more genes
    nsv5217222copy number variation1nstd204human GRCh37.p13 chr3: 60,333,132-61,384,674 , GRCh38.p13 chr3: 60,347,401-61,399,000 FHIT, TMED2P1, 7 more genes
    nsv5208853copy number variation1nstd204human GRCh38.p13 chr3: 60,717,233-60,752,204 , GRCh37.p13 chr3|NW_003871058.1: 144,635-179,606 , GRCh37.p13 chr3: 60,702,966-60,737,937 TMED2P1, PPIAP71, 1 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924467copy number variation1nstd200human GRCh38 chr3: 59,715,696-61,038,030 , GRCh37.p13 chr3: 59,701,422-61,023,702 MIR548BB, MTERF1P1, 9 more genes
    nsv4918518copy number variation1nstd200human GRCh38 chr3: 60,730,594-60,744,603 , GRCh37.p13 chr3: 60,716,327-60,730,336 , GRCh37.p13 chr3|NW_003871058.1: 157,996-172,005 PPIAP71, FHIT, 1 more genes
    nsv4918510copy number variation1nstd200human GRCh38 chr3: 60,551,470-60,799,426 , GRCh37.p13 chr3|NW_003871058.1: 1-226,828 , GRCh37.p13 chr3: 60,558,331-60,785,139 FHIT, TMED2P1, 4 more genes
    nsv4918505copy number variation1nstd200human GRCh38 chr3: 60,493,046-60,871,814 , GRCh37.p13 chr3|NW_003871058.1: 1-299,216 , GRCh37.p13 chr3: 60,558,332-60,857,486 FHIT, TMED2P1, 4 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4790913copy number variation1nstd200human GRCh37 chr3: 60,716,327-60,730,336 , GRCh38.p12 chr3: 60,730,594-60,744,603 TMED2P1, FHIT, 1 more genes
    nsv4790906copy number variation1nstd200human GRCh37 chr3: 60,537,203-60,785,139 , GRCh38.p12 chr3: 60,551,470-60,799,426 FHIT, TMED2P1, 4 more genes
    nsv4790901copy number variation1nstd200human GRCh37 chr3: 60,478,779-60,857,486 , GRCh38.p12 chr3: 60,493,046-60,871,814 FHIT, TMED2P1, 4 more genes
    nsv4790898copy number variation1nstd200human GRCh37 chr3: 60,446,094-60,953,869 , GRCh38.p12 chr3: 60,460,361-60,968,197 FHIT, TMED2P1, 4 more genes
    nsv4728491copy number variation1nstd102humanLikely benign GRCh37 chr3: 60,537,596-60,897,771 , GRCh38.p12 chr3: 60,551,863-60,912,099 FHIT, TMED2P1, 4 more genes
    nsv4680974copy number variation1nstd189human GRCh37.p13 chr3: 59,697,700-61,023,938 , GRCh38.p12 chr3: 59,711,974-61,038,266 FHIT, TMED2P1, 9 more genes
    nsv4680176copy number variation1nstd189human GRCh37.p13 chr3: 59,700,663-61,023,938 , GRCh38.p12 chr3: 59,714,937-61,038,266 FHIT, TMED2P1, 9 more genes
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