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Items: 1 to 20 of 364

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137751insertion1nstd232human GRCh37.p13 chr1: 220,749,346-220,749,346 , GRCh38.p12 chr1: 220,576,004-220,576,004 MARK1
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7095972copy number variation1nstd102humanPathogenic GRCh37 chr1: 218,520,044-220,986,760 , GRCh38.p12 chr1: 218,346,702-220,813,418 TGFB2, LOC105373475, 38 more genes
    nsv7095587copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,088,791-220,986,760 , GRCh38.p12 chr1: 219,915,449-220,813,418 BPNT1, SNORA36B, 24 more genes
    nsv7053947inversion1nstd229human GRCh38 chr1: 220,560,991-220,562,798 , GRCh37.p13 chr1: 220,734,333-220,736,140 MARK1
    nsv7052462inversion1nstd229human GRCh38 chr1: 219,653,745-221,511,784 , GRCh37.p13 chr1: 219,827,087-221,685,126 RNA5SP76, MIR215, 36 more genes
    nsv6677437copy number variation1nstd229human GRCh38 chr1: 220,536,754-220,590,649 , GRCh37.p13 chr1: 220,710,096-220,763,991 RN7SL464P, MARK1
    nsv6674627copy number variation1nstd229human GRCh38 chr1: 220,542,267-220,548,890 , GRCh37.p13 chr1: 220,715,609-220,722,232 MARK1
    nsv6670829copy number variation1nstd229human GRCh38 chr1: 220,555,601-220,684,900 , GRCh37.p13 chr1: 220,728,943-220,858,242 MARK1, HDAC1P2, 1 more genes
    nsv6665663copy number variation1nstd229human GRCh38 chr1: 220,543,582-220,543,797 , GRCh37.p13 chr1: 220,716,924-220,717,139 MARK1
    nsv6664040copy number variation1nstd229human GRCh38 chr1: 220,607,551-220,607,588 , GRCh37.p13 chr1: 220,780,893-220,780,930 MARK1
    nsv6662585copy number variation1nstd229human GRCh38 chr1: 220,632,401-220,662,900 , GRCh37.p13 chr1: 220,805,743-220,836,242 MARK1
    nsv6661412copy number variation1nstd229human GRCh38 chr1: 220,593,501-220,598,700 , GRCh37.p13 chr1: 220,766,843-220,772,042 MARK1
    nsv6659506copy number variation1nstd229human GRCh38 chr1: 220,535,281-220,539,955 , GRCh37.p13 chr1: 220,708,623-220,713,297 MARK1
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6547524inversion1nstd223human GRCh38 chr1: 220,546,982-220,547,700 , GRCh37.p13 chr1: 220,720,324-220,721,042 MARK1
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6335136copy number variation1nstd223human GRCh38 chr1: 220,643,614-220,648,515 , GRCh37.p13 chr1: 220,816,956-220,821,857 MARK1
    nsv6332640copy number variation1nstd223human GRCh38 chr1: 220,630,876-220,631,381 , GRCh37.p13 chr1: 220,804,218-220,804,723 MARK1
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