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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099248copy number variation1nstd231human GRCh38.p12 chr1: 172,685,012-173,856,229 , GRCh37 chr1: 172,654,152-173,825,367 TNFSF4, TNFSF18, 19 more genes
    nsv6644846copy number variation1nstd229human GRCh38 chr1: 172,689,801-173,072,375 , GRCh37.p13 chr1: 172,658,941-173,041,515 LOC107985225, SLC25A38P1, 3 more genes
    nsv6644798copy number variation1nstd229human GRCh38 chr1: 172,743,060-172,748,271 , GRCh37.p13 chr1: 172,712,200-172,717,411 SLC25A38P1
    nsv6644765copy number variation1nstd229human GRCh38 chr1: 171,564,330-172,954,419 , GRCh37.p13 chr1: 171,533,469-172,923,559 LOC107985225, RPS15P3, 27 more genes
    nsv6644717copy number variation1nstd229human GRCh38 chr1: 172,496,006-174,441,202 , GRCh37.p13 chr1: 172,465,146-174,410,340 RABGAP1L-DT, LOC100506023, 46 more genes
    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
    nsv6310765copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 171,605,065-173,962,123 , GRCh38.p12 chr1: 171,635,925-173,992,985 RNU6-157P, SNORD47, 60 more genes
    nsv6133940copy number variation1nstd213human GRCh37 chr1: 170,740,000-173,330,001 , GRCh38.p12 chr1: 170,770,859-173,360,862 TNFSF4, VAMP4, 50 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
    nsv6133600copy number variation1nstd213human GRCh37 chr1: 172,520,000-173,820,001 , GRCh38.p12 chr1: 172,550,860-173,850,863 FASLG, GOT2P2, 22 more genes
    nsv6133571copy number variation1nstd213human GRCh37 chr1: 172,670,000-173,070,001 , GRCh38.p12 chr1: 172,700,860-173,100,861 TNFSF18, SLC25A38P1, 3 more genes
    nsv6133567copy number variation1nstd213human GRCh37 chr1: 170,760,000-174,730,001 , GRCh38.p12 chr1: 170,790,859-174,760,863 FASLG, SERPINC1, 87 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
    nsv4683654copy number variation1nstd102humanUncertain significance GRCh37 chr1: 172,627,498-172,879,024 , GRCh38.p12 chr1: 172,658,358-172,909,884 AIMP1P2, LOC107985225, 3 more genes
    nsv4674768copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,430,471-174,635,618 , GRCh38.p12 chr1: 167,461,234-174,666,480 ATP1B1, RNU6-693P, 156 more genes
    nsv4436225copy number variation1nstd102humanPathogenic GRCh37 chr1: 172,652,343-183,538,289 , GRCh38.p12 chr1: 172,683,203-183,569,154 KIAA1614-AS1, LOC105371630, 190 more genes
    nsv4346686copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,423,492-180,367,623 , GRCh38.p12 chr1: 169,454,254-180,398,488 TNFSF4, MIR3119-1, 202 more genes
    nsv4346684copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189 LINC00626, RN7SL861P, 359 more genes
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