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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7053584inversion1nstd229human GRCh38 chr5: 144,534,922-150,861,041 , GRCh37.p13 chr5: 143,914,485-150,240,603 SMIM3, NAMPTP2, 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
    nsv7041990inversion1nstd229human GRCh38 chr5: 150,791,584-150,791,611 , GRCh37.p13 chr5: 150,171,146-150,171,173 SMIM3
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6796765copy number variation1nstd229human GRCh38 chr5: 150,796,901-150,802,000 , GRCh37.p13 chr5: 150,176,463-150,181,562 SMIM3
    nsv6794240copy number variation1nstd229human GRCh38 chr5: 150,783,341-150,785,976 , GRCh37.p13 chr5: 150,162,903-150,165,538 SMIM3
    nsv6791570copy number variation1nstd229human GRCh38 chr5: 150,752,801-150,807,500 , GRCh37.p13 chr5: 150,132,363-150,187,062 DCTN4, SMIM3
    nsv6778271copy number variation1nstd229human GRCh38 chr5: 150,790,722-150,811,313 , GRCh37.p13 chr5: 150,170,284-150,190,875 SMIM3
    nsv6630312copy number variation1nstd224human GRCh37 chr5: 150,167,118-150,282,735 , GRCh38.p12 chr5: 150,787,556-150,903,173 ZNF300, SMIM3, 1 more genes
    nsv6411312copy number variation1nstd223human GRCh38 chr5: 150,789,501-150,793,200 , GRCh37.p13 chr5: 150,169,063-150,172,762 SMIM3
    nsv6407534copy number variation1nstd223human GRCh38 chr5: 150,777,592-150,935,919 , GRCh37.p13 chr5: 150,157,154-150,315,481 SMIM3, ZNF300, 2 more genes
    nsv6404740copy number variation1nstd223human GRCh38 chr5: 150,797,201-150,805,200 , GRCh37.p13 chr5: 150,176,763-150,184,762 SMIM3
    nsv6402160copy number variation1nstd223human GRCh38 chr5: 150,796,801-150,801,800 , GRCh37.p13 chr5: 150,176,363-150,181,362 SMIM3
    nsv6397961copy number variation1nstd223human GRCh38 chr5: 150,795,901-150,802,700 , GRCh37.p13 chr5: 150,175,463-150,182,262 SMIM3
    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
    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
    nsv6068632insertion1nstd212human GRCh38 chr5: 150,784,568-150,784,568 , GRCh37.p13 chr5: 150,164,130-150,164,130 SMIM3
    nsv5720190mobile element insertion1nstd211human GRCh38 chr5: 150,794,129-150,794,129 , GRCh37.p13 chr5: 150,173,691-150,173,691 SMIM3
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