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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054431inversion1nstd229human GRCh38 chr4: 108,267,754-117,667,771 , GRCh37.p13 chr4: 109,188,910-118,588,926 , MIR297, 128 more genes
    nsv7050033inversion1nstd229human GRCh38 chr4: 115,977,874-117,255,646 , GRCh37.p13 chr4: 116,899,030-118,176,802 LOC105377385, TRMT112P1, 15 more genes
    nsv7043432inversion1nstd229human GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213 SEPTIN14P4, LINC02516, 109 more genes
    nsv7041573inversion1nstd229human GRCh38 chr4: 116,884,639-117,230,291 , GRCh37.p13 chr4: 117,805,795-118,151,447 LOC105377387, TRAM1L1, 2 more genes
    nsv6750772copy number variation1nstd229human GRCh38 chr4: 116,781,280-117,219,597 , GRCh37.p13 chr4: 117,702,436-118,140,753 TRAM1L1, LOC105377387, 4 more genes
    nsv6750546copy number variation1nstd229human GRCh38 chr4: 115,351,983-117,291,728 , GRCh37.p13 chr4: 116,273,139-118,212,884 LOC105377383, TRAM1L1, 18 more genes
    nsv6750000copy number variation1nstd229human GRCh38 chr4: 116,666,401-117,763,000 , GRCh37.p13 chr4: 117,587,557-118,684,155 NT5C3AP1, LINC02262, 10 more genes
    nsv6748353copy number variation1nstd229human GRCh38 chr4: 116,554,152-117,832,344 , GRCh37.p13 chr4: 117,475,308-118,753,499 RNU6-119P, HAVCR1P2, 12 more genes
    nsv6746801copy number variation1nstd229human GRCh38 chr4: 116,511,655-117,972,921 , GRCh37.p13 chr4: 117,432,811-118,894,076 RPSAP35, LOC105377388, 13 more genes
    nsv6573346inversion1nstd223human GRCh38 chr4: 116,884,639-117,230,294 , GRCh37.p13 chr4: 117,805,795-118,151,450 TRAM1L1, LOC105377387, 2 more genes
    nsv6572140inversion1nstd223human GRCh38 chr4: 108,267,752-117,667,773 , GRCh37.p13 chr4: 109,188,908-118,588,928 , RPS26P25, 128 more genes
    nsv6570561inversion1nstd223human GRCh38 chr4: 117,041,188-125,064,052 , GRCh37.p13 chr4: 117,962,344-125,985,207 MYOZ2, NT5C3AP1, 109 more genes
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6313750copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,888,785-129,649,979 , GRCh38.p12 chr4: 115,967,629-128,728,824 LOC105377395, SEPTIN7P14, 152 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6290265copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113 LOC105379404, IL21-AS1, 218 more genes
    nsv6135053copy number variation1nstd213human GRCh37 chr4: 117,710,000-119,370,001 , GRCh38.p12 chr4: 116,788,844-118,448,846 PRSS12, NDST3, 19 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv5969033inversion1nstd209human GRCh38 chr4: 108,267,752-117,667,772 , GRCh37.p13 chr4: 109,188,908-118,588,927 , ANK2, 134 more genes
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