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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv6636995copy number variation1nstd102humanUncertain significance GRCh37 chr4: 187,853,428-190,957,473 , GRCh38.p12 chr4: 186,932,274-190,036,318 LINC02515, LINC02514, 49 more genes
    nsv6636301copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,694,501-190,957,473 , GRCh38.p12 chr4: 182,773,348-190,036,318 LOC105377588, ENPP6, 139 more genes
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6634350copy number variation1nstd102humanPathogenic GRCh37 chr4: 185,211,271-190,957,473 , GRCh38.p12 chr4: 184,290,118-190,036,318 LINC02374, SLED1, 102 more genes
    nsv6394598copy number variation1nstd223human GRCh38 chr4: 190,011,739-190,047,565 , GRCh37.p13 chr4|NW_003571034.1: 104,669-140,495 , GRCh37.p13 chr4: 190,932,894-190,968,720 FRG2, RARRES2P4, 4 more genes
    nsv6393644copy number variation1nstd223human GRCh38 chr4: 190,009,478-190,044,211 , GRCh37.p13 chr4|NW_003571034.1: 102,408-137,141 , GRCh37.p13 chr4: 190,930,633-190,965,366 FRG2, RARRES2P4, 4 more genes
    nsv6383857copy number variation1nstd223human GRCh38 chr4: 190,010,382-190,050,504 , GRCh37.p13 chr4|NW_003571034.1: 103,312-143,434 , GRCh37.p13 chr4: 190,931,537-190,971,659 RNA5SP174, AGGF1P1, 4 more genes
    nsv6315348copy number variation1nstd102humanPathogenic GRCh37 chr4: 174,944,132-190,957,473 , GRCh38.p12 chr4: 174,022,981-190,036,318 SPATA4, ADAM20P2, 203 more genes
    nsv6315316copy number variation1nstd102humanLikely pathogenic GRCh38 chr4: 186,194,495-190,175,048 , GRCh37.p13 chr4: 187,115,649-190,828,225 F11, FAT1, 74 more genes
    nsv6313744copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,221,828-190,957,473 , GRCh38.p12 chr4: 182,300,675-190,036,318 RNU6-1053P, LINC02436, 141 more genes
    nsv6313663copy number variation1nstd102humanPathogenic GRCh37 chr4: 175,855,408-190,957,473 , GRCh38.p12 chr4: 174,934,257-190,036,318 LINC01596, NDUFB5P1, 190 more genes
    nsv6290964copy number variation1nstd102humanUncertain significance GRCh37 chr4: 189,828,191-190,957,473 , GRCh38.p12 chr4: 188,907,037-190,036,318 LINC01596, LOC105377611, 18 more genes
    nsv6290859copy number variation1nstd102humanUncertain significance GRCh37 chr4: 189,351,336-190,957,473 , GRCh38.p12 chr4: 188,430,182-190,036,318 RARRES2P4, LINC01262, 25 more genes
    nsv6141365copy number variation1nstd206human GRCh38 chr4: 189,977,381-190,093,000 , GRCh37.p13 chr4|NW_003571034.1: 70,311-185,930 , GRCh37.p13 chr4: 190,898,536-191,014,155 DUX4L9, DUX4L7, 15 more genes
    nsv6134927copy number variation1nstd213human GRCh37 chr4: 190,690,000-190,990,001 , GRCh38.p12 chr4: 189,768,846-190,068,846 FRG1, DUX4L8, 13 more genes
    nsv5473904copy number variation1nstd206human GRCh38 chr4: 190,024,381-190,041,381 , GRCh37.p13 chr4|NW_003571034.1: 117,311-134,311 , GRCh37.p13 chr4: 190,945,536-190,962,536 FRG2, RARRES2P4, 1 more genes
    nsv5226228copy number variation1nstd204human GRCh38.p13 chr4: 190,016,261-190,024,132 , GRCh37.p13 chr4: 190,937,416-190,945,287 , GRCh37.p13 chr4|NW_003571034.1: 109,191-117,062 RNA5SP175, FRG2, 1 more genes
    nsv5222102copy number variation1nstd204human GRCh38.p13 chr4: 190,027,101-190,042,500 , GRCh37.p13 chr4|NW_003571034.1: 120,031-135,430 , GRCh37.p13 chr4: 190,948,256-190,963,655 FRG2, RARRES2P4, 1 more genes
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