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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099250copy number variation1nstd231human GRCh38.p12 chr1: 174,623,673-177,335,804 , GRCh37 chr1: 174,592,811-177,304,940 ASTN1, TNR, 29 more genes
    nsv7053261inversion1nstd229human GRCh38 chr1: 175,779,844-176,419,349 , GRCh37.p13 chr1: 175,748,980-176,388,485 COP1, MORF4L1P7, 8 more genes
    nsv7044079inversion1nstd229human GRCh38 chr1: 174,711,171-179,623,233 , GRCh37.p13 chr1: 174,680,309-179,592,368 LOC100420262, RNU6-307P, 71 more genes
    nsv6645171copy number variation1nstd229human GRCh38 chr1: 175,753,637-175,985,166 , GRCh37.p13 chr1: 175,722,773-175,954,302 LINC01657, MIR1843, 4 more genes
    nsv6645121copy number variation1nstd229human GRCh38 chr1: 175,877,238-175,881,095 , GRCh37.p13 chr1: 175,846,374-175,850,231 LINC01657, LINC02803
    nsv6645120copy number variation1nstd229human GRCh38 chr1: 175,837,301-175,944,400 , GRCh37.p13 chr1: 175,806,437-175,913,536 COP1, RPS29P5, 2 more genes
    nsv6645036copy number variation1nstd229human GRCh38 chr1: 175,880,883-175,884,174 , GRCh37.p13 chr1: 175,850,019-175,853,310 LINC01657, LINC02803
    nsv6645030copy number variation1nstd229human GRCh38 chr1: 175,712,628-176,186,508 , GRCh37.p13 chr1: 175,681,764-176,155,644 RPS29P5, TNR, 5 more genes
    nsv6645015copy number variation1nstd229human GRCh38 chr1: 175,099,496-176,381,238 , GRCh37.p13 chr1: 175,068,632-176,350,374 RPS29P4, TNN, 13 more genes
    nsv6325372copy number variation1nstd223human GRCh38 chr1: 175,877,238-175,881,090 , GRCh37.p13 chr1: 175,846,374-175,850,226 LINC01657, LINC02803
    nsv6313519copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,881,608-175,899,893 , GRCh38.p12 chr1: 171,912,468-175,930,757 RNU6-693P, PIGC, 73 more genes
    nsv6289872copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,686,375-176,083,118 , GRCh37.p13 chr1: 173,655,514-176,052,254 ENTR1P2, GAS5-AS1, 49 more genes
    nsv6133949copy number variation1nstd213human GRCh37 chr1: 175,710,000-175,950,001 , GRCh38.p12 chr1: 175,740,864-175,980,865 TNR, COP1, 5 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133574copy number variation1nstd213human GRCh37 chr1: 175,010,000-176,860,001 , GRCh38.p12 chr1: 175,040,864-176,890,865 ASTN1, TNN, 17 more genes
    nsv6133573copy number variation1nstd213human GRCh37 chr1: 173,820,000-189,960,001 , GRCh38.p12 chr1: 173,850,862-189,990,871 ABL2, ASTN1, 235 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4728270copy number variation1nstd102humanUncertain significance GRCh37 chr1: 174,410,914-178,743,636 , GRCh38.p12 chr1: 174,441,776-178,774,501 LINC01741, MRPS14, 52 more genes
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