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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6716442copy number variation1nstd229human GRCh38 chr3: 71,748,101-71,828,900 , GRCh37.p13 chr3: 71,797,252-71,878,051 GPR27, EIF4E3, 3 more genes
    nsv6712385copy number variation1nstd229human GRCh38 chr3: 66,065,527-73,237,527 , GRCh37.p13 chr3: 66,051,202-73,286,678 , RNA5SP136, 79 more genes
    nsv6711975copy number variation1nstd229human GRCh38 chr3: 71,749,201-71,836,000 , GRCh37.p13 chr3: 71,798,352-71,885,151 LOC105377156, PROK2, 3 more genes
    nsv6375131copy number variation1nstd223human GRCh38 chr3: 71,750,301-71,755,400 , GRCh37.p13 chr3: 71,799,452-71,804,551 EIF4E3, GPR27
    nsv6373171copy number variation1nstd223human GRCh38 chr3: 71,752,401-71,755,000 , GRCh37.p13 chr3: 71,801,552-71,804,151 GPR27, EIF4E3
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5836786copy number variation1nstd209human GRCh38 chr3: 71,756,537-71,758,386 , GRCh37.p13 chr3: 71,805,688-71,807,537 GPR27
    nsv5564432copy number variation1nstd102humanPathogenic GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267 CCDC137P1, LOC105377160, 39 more genes
    nsv5227729copy number variation1nstd204human GRCh38.p13 chr3: 71,752,201-71,754,900 , GRCh37.p13 chr3: 71,801,352-71,804,051 GPR27, EIF4E3
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 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
    nsv4728221copy number variation1nstd102humanUncertain significance GRCh37 chr3: 70,938,608-74,660,846 , GRCh38.p12 chr3: 70,889,457-74,611,695 CCDC137P1, LINC02047, 45 more genes
    nsv4674193copy number variation1nstd102humanUncertain significance GRCh37 chr3: 71,665,558-72,020,026 , GRCh38.p12 chr3: 71,616,407-71,970,875 PROK2, LOC105377156, 4 more genes
    nsv4596610copy number variation1nstd183human GRCh37 chr3: 71,802,926-71,805,413 , GRCh38.p12 chr3: 71,753,775-71,756,262 EIF4E3, GPR27
    nsv4586679copy number variation1nstd183human GRCh37 chr3: 71,802,175-71,804,230 , GRCh38.p12 chr3: 71,753,024-71,755,079 GPR27, EIF4E3
    nsv4586593copy number variation1nstd183human GRCh37 chr3: 71,802,926-71,802,971 , GRCh38.p12 chr3: 71,753,775-71,753,820 EIF4E3, GPR27
    nsv4586592copy number variation1nstd183human GRCh37 chr3: 71,802,284-71,804,379 , GRCh38.p12 chr3: 71,753,133-71,755,228 GPR27, EIF4E3
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