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Items: 1 to 20 of 255

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145328copy number variation1nstd232human GRCh37.p13 chr5: 179,251,085-179,251,178 , GRCh38.p12 chr5: 179,824,085-179,824,178 , GRCh38.p12 chr5|NW_016107298.1: 589,640-589,733 SQSTM1
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7097138copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,260,567-179,263,593 , GRCh38.p12 chr5|NW_016107298.1: 599,127-602,153 , GRCh38.p12 chr5: 179,833,567-179,836,593 SQSTM1, MRNIP
    nsv7096770copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,413,111-179,263,593 , GRCh38.p12 chr5|NW_016107298.1: 1-602,153 , GRCh38.p12 chr5: 178,986,110-179,836,593 HMGB3P22, MAML1, 25 more genes
    nsv6797341copy number variation1nstd229human GRCh38 chr5: 179,830,489-179,844,669 , GRCh37.p13 chr5: 179,257,489-179,271,669 SQSTM1, RN7SKP150, 1 more genes
    nsv6797160copy number variation1nstd229human GRCh38 chr5: 179,793,991-179,804,648 , GRCh37.p13 chr5: 179,220,992-179,231,648 LTC4S, MGAT4B, 2 more genes
    nsv6796729copy number variation1nstd229human GRCh38 chr5: 179,814,640-179,817,033 , GRCh37.p13 chr5: 179,241,640-179,244,033 SQSTM1
    nsv6794347copy number variation1nstd229human GRCh38 chr5: 179,825,227-179,833,024 , GRCh37.p13 chr5: 179,252,227-179,260,024 SQSTM1
    nsv6786117copy number variation1nstd229human GRCh38 chr5: 179,803,021-180,143,476 , GRCh37.p13 chr5: 179,230,021-179,570,476 RASGEF1C, MIR340, 10 more genes
    nsv6782510copy number variation1nstd229human GRCh38 chr5: 179,835,062-179,837,594 , GRCh37.p13 chr5: 179,262,062-179,264,594 MRNIP, SQSTM1
    nsv6781410copy number variation1nstd229human GRCh38 chr5: 179,821,477-179,857,495 , GRCh37.p13 chr5: 179,248,477-179,284,495 SQSTM1, RN7SKP150, 2 more genes
    nsv6781077copy number variation1nstd229human GRCh38 chr5: 179,838,226-179,838,274 , GRCh37.p13 chr5: 179,265,226-179,265,274 SQSTM1, MRNIP
    nsv6780159copy number variation1nstd229human GRCh38 chr5: 179,820,704-180,383,099 , GRCh37.p13 chr5: 179,247,704-179,810,099 MAPK9, SQSTM1, 13 more genes
    nsv6779582copy number variation1nstd229human GRCh38 chr5: 179,833,782-179,836,432 , GRCh37.p13 chr5: 179,260,782-179,263,432 SQSTM1, MRNIP
    nsv6778685copy number variation1nstd229human GRCh38 chr5: 179,809,820-179,859,323 , GRCh37.p13 chr5: 179,236,820-179,286,323 RN7SKP150, MRNIP-DT, 2 more genes
    nsv6636440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,746,012-179,975,280 , GRCh38.p12 chr5: 178,319,011-180,548,280 RUFY1-AS1, RPS15AP18, 60 more genes
    nsv6636392copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,947,702-179,645,244 , GRCh38.p12 chr5: 179,520,701-180,218,244 , GRCh38.p12 chr5|NW_016107298.1: 285,253-673,059 LOC646058, LOC100289470, 26 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6313896copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,860,745-179,534,363 , GRCh38.p12 chr5: 179,433,744-180,107,363 , GRCh38.p12 chr5|NW_016107298.1: 198,326-673,059 RUFY1, HNRNPH1, 27 more genes
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