U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 146

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    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
    nsv6791052copy number variation1nstd229human GRCh38 chr5: 179,796,811-179,801,991 , GRCh37.p13 chr5: 179,223,812-179,228,991 LTC4S, MIR1229, 1 more genes
    nsv6784088copy number variation1nstd229human GRCh38 chr5: 179,782,504-179,793,089 , GRCh37.p13 chr5: 179,209,505-179,220,090 LOC100884169, LTC4S
    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
    nsv6313755copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,954,576-180,198,875 , GRCh38.p12 chr5: 178,527,575-180,771,875 MIR340, RASGEF1C, 64 more genes
    nsv6313609copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,082,801-179,409,280 , GRCh38.p12 chr5|NW_016107298.1: 421,507-673,059 , GRCh38.p12 chr5: 179,655,800-179,982,280 CANX, RN7SKP150, 15 more genes
    nsv6135399copy number variation1nstd213human GRCh37 chr5: 178,600,000-179,310,001 , GRCh38.p12 chr5: 179,172,999-179,883,001 , GRCh38.p12 chr5|NW_016107298.1: 1-648,561 SQSTM1, MAML1, 24 more genes
    nsv6135397copy number variation1nstd213human GRCh37 chr5: 176,330,000-179,310,001 , GRCh38.p12 chr5: 176,902,999-179,883,001 CANX, DBN1, 95 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135136copy number variation1nstd213human GRCh37 chr5: 178,930,000-179,330,001 , GRCh38.p12 chr5: 179,502,999-179,903,001 , GRCh38.p12 chr5|NW_016107298.1: 267,638-668,561 CANX, HNRNPH1, 21 more genes
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5381440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,699,902-179,263,603 , GRCh38.p12 chr5: 179,272,901-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 37,608-602,163 LOC105377762, LOC105377759, 21 more genes
    nsv5381377copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,770,758-179,263,603 , GRCh38.p12 chr5: 179,343,757-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 108,464-602,163 LOC100502572, C5orf60, 21 more genes
    nsv5301596copy number variation1nstd204human GRCh38.p13 chr5: 179,616,292-180,442,361 , GRCh37.p13 chr5: 179,043,293-179,869,361 MIR1229, MAPK9, 25 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center