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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5462109copy number variation1nstd206human GRCh38 chr4: 175,785,135-176,386,595 , GRCh37.p13 chr4: 176,706,286-177,307,746 GPM6A, SPCS3, 6 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4729375copy number variation1nstd102humanPathogenic GRCh37 chr4: 169,108,358-184,425,536 , GRCh38.p12 chr4: 168,187,207-183,504,383 GALNT7-DT, LOC105377524, 154 more genes
    nsv4674400copy number variation1nstd102humanUncertain significance GRCh37 chr4: 176,916,599-177,346,411 , GRCh38.p12 chr4: 175,995,448-176,425,260 ASB5, GPM6A, 4 more genes
    nsv4674043copy number variation1nstd102humanPathogenic GRCh37 chr4: 165,010,461-190,957,473 , GRCh38.p12 chr4: 164,089,309-190,036,318 CYP4V2, ZFP42, 319 more genes
    nsv4457244copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,174,061-190,957,473 , GRCh38.p12 chr4: 150,252,909-190,036,318 LOC105377509, MIR3140, 487 more genes
    nsv4457131copy number variation1nstd102humanPathogenic GRCh37 chr4: 165,069,355-177,189,728 , GRCh38.p12 chr4: 164,148,203-176,268,577 LINC02269, NOL8P1, 140 more genes
    nsv4456536copy number variation1nstd102humanUncertain significance GRCh37 chr4: 176,868,072-177,282,029 , GRCh38.p12 chr4: 175,946,921-176,360,878 WDR17, ASB5, 5 more genes
    nsv4456171copy number variation1nstd102humanPathogenic GRCh37 chr4: 166,623,890-190,957,473 , GRCh38.p12 chr4: 165,702,738-190,036,318 TRIML2, LTO1P1, 284 more genes
    nsv4455968copy number variation1nstd102humanPathogenic GRCh37 chr4: 169,607,746-190,957,473 , GRCh38.p12 chr4: 168,686,595-190,036,318 LOC105377565, LOC105377568, 266 more genes
    nsv4455301copy number variation1nstd102humanPathogenic GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509 SMARCA5, SFRP2, 633 more genes
    nsv4436340copy number variation1nstd102humanPathogenic GRCh37 chr4: 171,316,973-180,632,505 , GRCh38.p12 chr4: 170,395,822-179,711,352 ADAM29, GALNTL6, 84 more genes
    nsv4348053copy number variation1nstd102humanPathogenic GRCh37 chr4: 171,663,620-190,431,429 , GRCh38.p12 chr4: 170,742,469-189,510,275 LOC132386, DCTD, 224 more genes
    nsv4347789copy number variation1nstd102humanPathogenic GRCh37 chr4: 174,610,492-190,427,545 , GRCh38.p12 chr4: 173,689,341-189,506,391 RNU6-1053P, LINC02436, 193 more genes
    nsv3924008copy number variation1nstd102humanPathogenic GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788 PPID, METTL14-DT, 828 more genes
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