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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
    nsv6644882copy number variation1nstd229human GRCh38 chr1: 173,606,128-173,614,971 , GRCh37.p13 chr1: 173,575,267-173,584,110 ANKRD45, TEX50
    nsv6644824copy number variation1nstd229human GRCh38 chr1: 173,628,970-173,662,459 , GRCh37.p13 chr1: 173,598,109-173,631,598 LOC105371619, ANKRD45, 1 more genes
    nsv6644823copy number variation1nstd229human GRCh38 chr1: 173,618,388-173,672,281 , GRCh37.p13 chr1: 173,587,527-173,641,420 ANKRD45, LOC105371619, 1 more genes
    nsv6644822copy number variation1nstd229human GRCh38 chr1: 173,611,017-173,619,526 , GRCh37.p13 chr1: 173,580,156-173,588,665 ANKRD45, TEX50
    nsv6644754copy number variation1nstd229human GRCh38 chr1: 173,627,201-173,648,500 , GRCh37.p13 chr1: 173,596,340-173,617,639 ANKRD45, TEX50, 1 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
    nsv6644376copy number variation1nstd229human GRCh38 chr1: 173,587,361-173,612,549 , GRCh37.p13 chr1: 173,556,500-173,581,688 SLC9C2, ANKRD45, 1 more genes
    nsv6327929copy number variation1nstd223human GRCh38 chr1: 173,588,688-173,613,788 , GRCh37.p13 chr1: 173,557,827-173,582,927 TEX50, SLC9C2, 1 more genes
    nsv6319201copy number variation1nstd223human GRCh38 chr1: 173,606,127-173,614,971 , GRCh37.p13 chr1: 173,575,266-173,584,110 TEX50, ANKRD45
    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
    nsv6289986copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,501,975-175,305,010 , GRCh37.p13 chr1: 173,471,114-175,274,146 GAS5-AS1, ENTR1P2, 44 more genes
    nsv6289891copy number variation1nstd102humanPathogenic GRCh38 chr1: 172,987,296-174,843,232 , GRCh37.p13 chr1: 172,956,436-174,812,370 LOC100302291, SNORD75, 41 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
    nsv6133749copy number variation1nstd213human GRCh37 chr1: 173,530,000-175,550,001 , GRCh38.p12 chr1: 173,560,861-175,580,865 SERPINC1, KIAA0040, 46 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
    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
    nsv6055178insertion1nstd212human GRCh38 chr1: 173,613,104-173,613,104 , GRCh37.p13 chr1: 173,582,243-173,582,243 TEX50, ANKRD45
    nsv5981762copy number variation1nstd212human GRCh38 chr1: 173,608,839-173,608,937 , GRCh37.p13 chr1: 173,577,978-173,578,076 TEX50, ANKRD45
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