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Items: 1 to 20 of 85

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097521copy number variation1nstd102humanPathogenic GRCh37 chr5: 172,659,748-172,666,091 , GRCh38.p12 chr5: 173,232,745-173,239,088 NKX2-5
    nsv7097134copy number variation1nstd102humanPathogenic GRCh37 chr5: 172,089,144-172,774,583 , GRCh38.p12 chr5: 172,662,141-173,347,580 RNA5SP200, MIR5003, 22 more genes
    nsv7096766copy number variation1nstd102humanPathogenic GRCh37 chr5: 172,657,631-172,661,899 , GRCh38.p12 chr5: 173,230,628-173,234,896 NKX2-5
    nsv7096765copy number variation1nstd102humanUncertain significance GRCh37 chr5: 171,765,373-172,939,426 , GRCh38.p12 chr5: 172,338,369-173,512,423 MIR5003, LOC285591, 31 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
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6797237copy number variation1nstd229human GRCh38 chr5: 173,140,401-173,386,000 , GRCh37.p13 chr5: 172,567,404-172,813,003 STC2, BNIP1, 8 more genes
    nsv6792770copy number variation1nstd229human GRCh38 chr5: 173,231,366-173,354,838 , GRCh37.p13 chr5: 172,658,369-172,781,841 MIR8056, MIR12118, 4 more genes
    nsv6787855copy number variation1nstd229human GRCh38 chr5: 173,232,901-173,238,800 , GRCh37.p13 chr5: 172,659,904-172,665,803 NKX2-5
    nsv6782955copy number variation1nstd229human GRCh38 chr5: 172,218,701-173,333,400 , GRCh37.p13 chr5: 171,645,705-172,760,403 ATP6V0E1, MIR10523, 31 more genes
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    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
    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
    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
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5897866copy number variation1nstd209human GRCh38 chr5: 173,235,710-173,236,889 , GRCh37.p13 chr5: 172,662,713-172,663,892 NKX2-5
    nsv5842131copy number variation1nstd209human GRCh38 chr5: 173,235,816-173,236,944 , GRCh37.p13 chr5: 172,662,819-172,663,947 NKX2-5
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
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