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Items: 1 to 20 of 191

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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
    nsv7095973copy number variation1nstd102humanPathogenic GRCh37 chr1: 220,088,791-220,445,679 , GRCh38.p12 chr1: 219,915,449-220,272,337 AURKAP1, IARS2, 13 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
    nsv7095512copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,088,791-220,406,225 , GRCh38.p12 chr1: 219,915,449-220,232,883 MIR215, SNX2P1, 11 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
    nsv7040510inversion1nstd229human GRCh38 chr1: 220,115,348-220,117,979 , GRCh37.p13 chr1: 220,288,690-220,291,321 MIR194-1, MIR215, 1 more genes
    nsv6674937copy number variation1nstd229human GRCh38 chr1: 220,115,301-220,120,400 , GRCh37.p13 chr1: 220,288,643-220,293,742 IARS2, MIR215, 1 more genes
    nsv6670619copy number variation1nstd229human GRCh38 chr1: 220,115,501-220,120,400 , GRCh37.p13 chr1: 220,288,843-220,293,742 MIR215, MIR194-1, 1 more genes
    nsv6669144copy number variation1nstd229human GRCh38 chr1: 220,115,347-220,117,986 , GRCh37.p13 chr1: 220,288,689-220,291,328 IARS2, MIR215, 1 more genes
    nsv6659061copy number variation1nstd229human GRCh38 chr1: 220,052,331-220,322,940 , GRCh37.p13 chr1: 220,225,673-220,496,282 AURKAP1, RPS15AP12, 12 more genes
    nsv6658142copy number variation1nstd229human GRCh38 chr1: 220,012,601-220,117,900 , GRCh37.p13 chr1: 220,185,943-220,291,242 IARS2, LOC105373475, 4 more genes
    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
    nsv6626166copy number variation1nstd224human GRCh37 chr1: 219,636,541-220,636,032 , GRCh38.p12 chr1: 219,463,199-220,462,690 MORF4L1P1, MIR215, 19 more genes
    nsv6555384inversion1nstd223human GRCh38 chr1: 219,848,358-220,334,963 , GRCh37.p13 chr1: 220,021,700-220,508,305 MIR215, RPLP0P5, 16 more genes
    nsv6542432inversion1nstd223human GRCh38 chr1: 220,117,978-220,118,317 , GRCh37.p13 chr1: 220,291,320-220,291,659 IARS2, MIR194-1, 1 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
    nsv6332302copy number variation1nstd223human GRCh38 chr1: 220,115,346-220,117,986 , GRCh37.p13 chr1: 220,288,688-220,291,328 IARS2, MIR215, 1 more genes
    nsv6329061copy number variation1nstd223human GRCh38 chr1: 220,115,501-220,120,400 , GRCh37.p13 chr1: 220,288,843-220,293,742 IARS2, MIR215, 1 more genes
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