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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7052462inversion1nstd229human GRCh38 chr1: 219,653,745-221,511,784 , GRCh37.p13 chr1: 219,827,087-221,685,126 RNA5SP76, MIR215, 36 more genes
    nsv6676337copy number variation1nstd229human GRCh38 chr1: 220,776,408-220,779,735 , GRCh37.p13 chr1: 220,949,750-220,953,077 MTARC2
    nsv6670816copy number variation1nstd229human GRCh38 chr1: 220,762,818-220,767,763 , GRCh37.p13 chr1: 220,936,160-220,941,105 MTARC2
    nsv6670394copy number variation1nstd229human GRCh38 chr1: 220,737,567-220,749,372 , GRCh37.p13 chr1: 220,910,909-220,922,714 MTARC2
    nsv6667074copy number variation1nstd229human GRCh38 chr1: 220,752,088-220,783,140 , GRCh37.p13 chr1: 220,925,430-220,956,482 MTARC2
    nsv6666027copy number variation1nstd229human GRCh38 chr1: 220,746,301-220,790,400 , GRCh37.p13 chr1: 220,919,643-220,963,742 MTARC2, MTARC1
    nsv6665846copy number variation1nstd229human GRCh38 chr1: 220,723,171-220,788,956 , GRCh37.p13 chr1: 220,896,513-220,962,298 MTARC1, MTARC2
    nsv6662727copy number variation1nstd229human GRCh38 chr1: 220,781,273-220,787,434 , GRCh37.p13 chr1: 220,954,615-220,960,776 MTARC2, MTARC1
    nsv6661898copy number variation1nstd229human GRCh38 chr1: 220,757,404-220,848,174 , GRCh37.p13 chr1: 220,930,746-221,021,516 HLX-AS1, LINC01352, 3 more genes
    nsv6661633copy number variation1nstd229human GRCh38 chr1: 220,750,443-220,756,535 , GRCh37.p13 chr1: 220,923,785-220,929,877 MTARC2
    nsv6660276copy number variation1nstd229human GRCh38 chr1: 220,764,147-220,766,565 , GRCh37.p13 chr1: 220,937,489-220,939,907 MTARC2
    nsv6659631copy number variation1nstd229human GRCh38 chr1: 220,757,470-220,760,612 , GRCh37.p13 chr1: 220,930,812-220,933,954 MTARC2
    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
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6539689inversion1nstd223human GRCh38 chr1: 220,764,185-220,764,747 , GRCh37.p13 chr1: 220,937,527-220,938,089 MTARC2
    nsv6333028copy number variation1nstd223human GRCh38 chr1: 220,776,408-220,779,732 , GRCh37.p13 chr1: 220,949,750-220,953,074 MTARC2
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