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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096974copy number variation1nstd102humanUncertain significance GRCh37 chr4: 121,616,266-124,323,706 , GRCh38.p12 chr4: 120,695,111-123,402,551 RN7SL335P, QRFPR, 40 more genes
    nsv7046858inversion1nstd229human GRCh38 chr4: 120,026,051-121,477,397 , GRCh37.p13 chr4: 120,947,206-122,398,552 RN7SKP137, LOC107986309, 14 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
    nsv6750472copy number variation1nstd229human GRCh38 chr4: 121,413,101-121,477,400 , GRCh37.p13 chr4: 122,334,256-122,398,555 TUBB4BP5, LOC107986309
    nsv6748767copy number variation1nstd229human GRCh38 chr4: 121,412,599-121,474,456 , GRCh37.p13 chr4: 122,333,754-122,395,611 TUBB4BP5, LOC107986309
    nsv6743154copy number variation1nstd229human GRCh38 chr4: 121,413,093-121,474,459 , GRCh37.p13 chr4: 122,334,248-122,395,614 TUBB4BP5, LOC107986309
    nsv6742186copy number variation1nstd229human GRCh38 chr4: 121,412,801-121,478,700 , GRCh37.p13 chr4: 122,333,956-122,399,855 TUBB4BP5, LOC107986309
    nsv6741644copy number variation1nstd229human GRCh38 chr4: 121,450,094-121,450,671 , GRCh37.p13 chr4: 122,371,249-122,371,826 TUBB4BP5, LOC107986309
    nsv6570561inversion1nstd223human GRCh38 chr4: 117,041,188-125,064,052 , GRCh37.p13 chr4: 117,962,344-125,985,207 MYOZ2, NT5C3AP1, 109 more genes
    nsv6381383copy number variation1nstd223human GRCh38 chr4: 121,413,093-121,474,455 , GRCh37.p13 chr4: 122,334,248-122,395,610 TUBB4BP5, LOC107986309
    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
    nsv6134886copy number variation1nstd213human GRCh37 chr4: 121,830,000-124,220,001 , GRCh38.p12 chr4: 120,908,845-123,298,846 ANXA5, CCNA2, 36 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
    nsv6069928insertion1nstd212human GRCh38 chr4: 121,452,105-121,452,105 , GRCh37.p13 chr4: 122,373,260-122,373,260 TUBB4BP5, LOC107986309
    nsv5956640insertion1nstd209human GRCh38 chr4: 121,452,105-121,452,105 , GRCh37.p13 chr4: 122,373,260-122,373,260 TUBB4BP5, LOC107986309
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
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