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Items: 1 to 20 of 412

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7098857copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,245,868-39,700,010 , GRCh38.p12 chr4: 39,244,248-39,698,390 UGDH, UBE2K, 13 more genes
    nsv7097250copy number variation1nstd102humanPathogenic GRCh37 chr4: 39,218,734-39,219,745 , GRCh38.p12 chr4: 39,217,114-39,218,125 WDR19
    nsv7097249copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,187,326-39,478,735 , GRCh38.p12 chr4: 39,185,706-39,477,115 RNU6-32P, RNU6-887P, 6 more genes
    nsv7097248copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,184,178-39,259,194 , GRCh38.p12 chr4: 39,182,558-39,257,574 WDR19
    nsv7096850copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,226,484-39,226,673 , GRCh38.p12 chr4: 39,224,864-39,225,053 WDR19
    nsv7096849copy number variation1nstd102humanUncertain significance GRCh37 chr4: 38,765,721-39,478,735 , GRCh38.p12 chr4: 38,764,100-39,477,115 TMEM156, TLR6, 14 more genes
    nsv7096730copy number variation1nstd102humanPathogenic GRCh37 chr4: 39,216,201-39,218,880 , GRCh38.p12 chr4: 39,214,581-39,217,260 WDR19
    nsv7049186inversion1nstd229human GRCh38 chr4: 38,135,041-40,245,309 , GRCh37.p13 chr4: 38,136,662-40,246,929 SMIM14, RNU6-887P, 42 more genes
    nsv7038584inversion1nstd229human GRCh38 chr4: 38,474,718-40,416,508 , GRCh37.p13 chr4: 38,476,339-40,418,525 RPL9, UBE2K, 41 more genes
    nsv6737120copy number variation1nstd229human GRCh38 chr4: 39,258,644-39,262,364 , GRCh37.p13 chr4: 39,260,264-39,263,984 WDR19
    nsv6736675copy number variation1nstd229human GRCh38 chr4: 39,195,093-39,198,303 , GRCh37.p13 chr4: 39,196,713-39,199,923 WDR19
    nsv6734359copy number variation1nstd229human GRCh38 chr4: 39,230,901-39,308,100 , GRCh37.p13 chr4: 39,232,521-39,309,720 RFC1, RNU6-32P, 1 more genes
    nsv6732169copy number variation1nstd229human GRCh38 chr4: 39,256,701-39,308,800 , GRCh37.p13 chr4: 39,258,321-39,310,420 WDR19, RFC1, 1 more genes
    nsv6731771copy number variation1nstd229human GRCh38 chr4: 39,033,924-39,356,182 , GRCh37.p13 chr4: 39,035,544-39,357,802 RFC1, LOC105374418, 3 more genes
    nsv6729911copy number variation1nstd229human GRCh38 chr4: 39,243,316-39,257,862 , GRCh37.p13 chr4: 39,244,936-39,259,482 WDR19
    nsv6727781copy number variation1nstd229human GRCh38 chr4: 39,220,375-39,232,339 , GRCh37.p13 chr4: 39,221,995-39,233,959 WDR19
    nsv6727045copy number variation1nstd229human GRCh38 chr4: 39,286,031-39,286,099 , GRCh37.p13 chr4: 39,287,651-39,287,719 RFC1, WDR19
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