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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046899inversion1nstd229human GRCh38 chr4: 118,146,331-118,464,228 , GRCh37.p13 chr4: 119,067,486-119,385,383 NDST3, FKBP4P1, 5 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
    nsv6754245copy number variation1nstd229human GRCh38 chr4: 118,193,147-118,653,405 , GRCh37.p13 chr4: 119,114,302-119,574,560 CICP16, LOC105377392, 11 more genes
    nsv6750651copy number variation1nstd229human GRCh38 chr4: 118,277,101-118,279,100 , GRCh37.p13 chr4: 119,198,256-119,200,255 PRSS12, SNORA24, 1 more genes
    nsv6738825copy number variation1nstd229human GRCh38 chr4: 118,276,692-118,276,875 , GRCh37.p13 chr4: 119,197,847-119,198,030 SNHG8
    nsv6738216copy number variation1nstd229human GRCh38 chr4: 118,146,301-118,579,300 , GRCh37.p13 chr4: 119,067,456-119,500,455 SNORA24, NDUFS5P5, 7 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
    nsv6379848copy number variation1nstd223human GRCh38 chr4: 118,193,140-118,653,403 , GRCh37.p13 chr4: 119,114,295-119,574,558 SEPTIN14P4, RNU6-1054P, 11 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
    nsv6140487copy number variation1nstd206human GRCh38 chr4: 117,605,381-118,619,381 , GRCh37.p13 chr4: 118,526,536-119,540,536 SNORA24, LINC02264, 13 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
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv4943903copy number variation1nstd200human GRCh38 chr4: 118,193,133-118,653,407 , GRCh37.p13 chr4: 119,114,288-119,574,562 SNORA24, LOC729218, 11 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
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