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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7057944inversion1nstd229human GRCh38 chr5: 172,134,356-176,589,266 , GRCh37.p13 chr5: 171,561,360-176,016,267 MIR10523, NIFKP2, 92 more genes
    nsv7040659inversion1nstd229human GRCh38 chr5: 174,927,732-178,443,561 , GRCh37.p13 chr5: 174,354,735-177,870,562 RN7SKP148, FAM193B-DT, 90 more genes
    nsv7040096inversion1nstd229human GRCh38 chr5: 175,807,694-175,811,135 , GRCh37.p13 chr5: 175,234,697-175,238,138 CPLX2
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6796221copy number variation1nstd229human GRCh38 chr5: 175,838,401-175,845,800 , GRCh37.p13 chr5: 175,265,404-175,272,803 CPLX2
    nsv6794562copy number variation1nstd229human GRCh38 chr5: 175,865,261-175,877,494 , GRCh37.p13 chr5: 175,292,264-175,304,497 CPLX2
    nsv6794405copy number variation1nstd229human GRCh38 chr5: 175,860,258-175,871,347 , GRCh37.p13 chr5: 175,287,261-175,298,350 CPLX2
    nsv6793858copy number variation1nstd229human GRCh38 chr5: 175,803,877-175,885,244 , GRCh37.p13 chr5: 175,230,880-175,312,247 LOC105377744, CPLX2
    nsv6789920copy number variation1nstd229human GRCh38 chr5: 175,856,233-175,862,742 , GRCh37.p13 chr5: 175,283,236-175,289,745 CPLX2
    nsv6784896copy number variation1nstd229human GRCh38 chr5: 175,862,285-175,862,655 , GRCh37.p13 chr5: 175,289,288-175,289,658 CPLX2
    nsv6783470copy number variation1nstd229human GRCh38 chr5: 175,880,736-175,881,783 , GRCh37.p13 chr5: 175,307,739-175,308,786 CPLX2
    nsv6780606copy number variation1nstd229human GRCh38 chr5: 175,857,424-175,905,089 , GRCh37.p13 chr5: 175,284,427-175,332,092 CPLX2
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6630497copy number variation1nstd224human GRCh37 chr5: 175,176,876-175,273,481 , GRCh38.p12 chr5: 175,749,873-175,846,478 LOC105377744, CPLX2
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6300349copy number variation1nstd186human GRCh37 chr5: 175,255,523-175,257,588 , GRCh38.p12 chr5: 175,828,520-175,830,585 CPLX2
    nsv6295639copy number variation1nstd186human GRCh37 chr5: 175,293,978-175,294,263 , GRCh38.p12 chr5: 175,866,975-175,867,260 CPLX2
    nsv6136933translocation1nstd213human GRCh37 chr5: 175,261,812-175,261,812 , GRCh37 chr5: 175,933,058-175,933,058 , GRCh38.p12 chr5: 175,834,809-175,834,809 , GRCh38.p12 chr5: 176,506,057-176,506,057 CPLX2, FAF2
    nsv6136101copy number variation1nstd213human GRCh37 chr5: 174,560,000-175,290,001 , GRCh38.p12 chr5: 175,132,997-175,862,998 DRD1, HRH2, 7 more genes
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