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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7055902inversion1nstd229human GRCh38 chr1: 36,155,822-36,482,474 , GRCh37.p13 chr1: 36,621,423-36,948,075 UBE2V2P4, RNU4-27P, 13 more genes
    nsv7053057inversion1nstd229human GRCh38 chr1: 36,474,150-36,541,660 , GRCh37.p13 chr1: 36,939,751-37,007,261 CSF3R
    nsv7046918inversion1nstd229human GRCh38 chr1: 34,689,928-38,980,899 , GRCh37.p13 chr1: 35,155,529-39,446,571 LOC105378647, NCDN, 112 more genes
    nsv7046389inversion1nstd229human GRCh38 chr1: 31,492,639-36,569,102 , GRCh37.p13 chr1: 32,017,064-37,034,703 LOC105378642, TMEM35B, 127 more genes
    nsv7040332inversion1nstd229human GRCh38 chr1: 34,936,903-38,057,517 , GRCh37.p13 chr1: 35,402,504-38,523,189 MAP7D1, RPL12P45, 83 more genes
    nsv6649529copy number variation1nstd229human GRCh38 chr1: 36,475,433-36,520,898 , GRCh37.p13 chr1: 36,941,034-36,986,499 CSF3R
    nsv6649479copy number variation1nstd229human GRCh38 chr1: 36,481,408-36,481,578 , GRCh37.p13 chr1: 36,947,009-36,947,179 CSF3R
    nsv6649477copy number variation1nstd229human GRCh38 chr1: 36,434,444-36,466,247 , GRCh37.p13 chr1: 36,900,045-36,931,848 LOC107984940, MRPS15, 2 more genes
    nsv6649466copy number variation1nstd229human GRCh38 chr1: 36,062,801-36,545,100 , GRCh37.p13 chr1: 36,528,402-37,010,701 ADPRS, TEKT2, 18 more genes
    nsv6649462copy number variation1nstd229human GRCh38 chr1: 35,975,501-36,714,600 , GRCh37.p13 chr1: 36,441,102-37,180,201 LSM10, LOC105378648, 22 more genes
    nsv6649328copy number variation1nstd229human GRCh38 chr1: 36,468,801-36,472,800 , GRCh37.p13 chr1: 36,934,402-36,938,401 CSF3R
    nsv6649327copy number variation1nstd229human GRCh38 chr1: 36,466,735-36,466,994 , GRCh37.p13 chr1: 36,932,336-36,932,595 CSF3R
    nsv6636592copy number variation1nstd102humanPathogenic GRCh37 chr1: 35,104,233-37,357,913 , GRCh38.p12 chr1: 34,638,632-36,892,312 EFCAB14P1, SNORA63C, 56 more genes
    nsv6550791inversion1nstd223human GRCh38 chr1: 36,477,417-36,478,565 , GRCh37.p13 chr1: 36,943,018-36,944,166 CSF3R
    nsv6313765copy number variation1nstd102humanUncertain significance GRCh37 chr1: 36,041,366-39,112,237 , GRCh38.p12 chr1: 35,575,765-38,646,565 RNU6-510P, AGO3, 78 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6310961copy number variation1nstd102humanUncertain significance GRCh37 chr1: 36,940,958-36,941,294 , GRCh38.p12 chr1: 36,475,357-36,475,693 CSF3R
    nsv6133869copy number variation1nstd213human GRCh37 chr1: 33,400,000-36,950,001 , GRCh38.p12 chr1: 32,934,399-36,484,400 AK2, COL8A2, 77 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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