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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142278insertion1nstd232human GRCh37.p13 chr5: 150,483,251-150,483,251 , GRCh38.p12 chr5: 151,103,690-151,103,690 ANXA6
    nsv7056886inversion1nstd229human GRCh38 chr5: 151,132,067-151,132,090 , GRCh37.p13 chr5: 150,511,628-150,511,651 ANXA6
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6792747copy number variation1nstd229human GRCh38 chr5: 151,002,201-151,187,400 , GRCh37.p13 chr5: 150,381,763-150,566,961 LOC107986463, LOC105378228, 4 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
    nsv6574458inversion1nstd223human GRCh38 chr5: 151,111,819-151,112,802 , GRCh37.p13 chr5: 150,491,380-150,492,363 ANXA6
    nsv6566708inversion1nstd223human GRCh38 chr5: 151,149,564-151,150,005 , GRCh37.p13 chr5: 150,529,125-150,529,566 ANXA6
    nsv6412266copy number variation1nstd223human GRCh38 chr5: 151,115,413-151,115,676 , GRCh37.p13 chr5: 150,494,974-150,495,237 ANXA6
    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
    nsv6256301mobile element insertion1nstd215human GRCh38 chr5: 151,154,752-151,154,752 , GRCh37.p13 chr5: 150,534,313-150,534,313 ANXA6
    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
    nsv6135120copy number variation1nstd213human GRCh37 chr5: 143,910,000-152,670,001 , GRCh38.p12 chr5: 144,530,437-153,290,441 ADRB2, ANXA6, 143 more genes
    nsv6012089copy number variation1nstd212human GRCh38 chr5: 151,141,676-151,141,729 , GRCh37.p13 chr5: 150,521,237-150,521,290 ANXA6
    nsv6002212copy number variation1nstd212human GRCh38 chr5: 151,103,027-151,103,106 , GRCh37.p13 chr5: 150,482,588-150,482,667 ANXA6
    nsv5952469insertion1nstd209human GRCh38 chr5: 151,140,577-151,140,577 , GRCh37.p13 chr5: 150,520,138-150,520,138 ANXA6
    nsv5538953insertion1nstd206human GRCh38 chr5: 151,140,577-151,140,577 , GRCh37.p13 chr5: 150,520,138-150,520,138 ANXA6
    nsv5236828copy number variation1nstd204human GRCh38.p13 chr5: 151,101,069-151,102,599 , GRCh37.p13 chr5: 150,480,630-150,482,160 ANXA6
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
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