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Items: 1 to 20 of 171

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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
    nsv5315801copy number variation1nstd204human GRCh38.p13 chr4: 174,523,283-174,568,054 , GRCh37.p13 chr4: 175,444,434-175,489,205 HPGD, LOC105377548, 1 more genes
    nsv5235183copy number variation1nstd204human GRCh38.p13 chr4: 174,523,034-174,556,804 , GRCh37.p13 chr4: 175,444,185-175,477,955 LOC105377548, HPGD, 1 more genes
    nsv4944062copy number variation1nstd200human GRCh38 chr4: 173,724,041-174,933,391 , GRCh37.p13 chr4: 174,645,192-175,854,542 LOC107986204, LOC101928551, 16 more genes
    nsv4794692copy number variation1nstd200human GRCh37 chr4: 175,444,444-175,489,199 , GRCh38.p12 chr4: 174,523,293-174,568,048 HPGD, LOC100419741, 1 more genes
    nsv4794687copy number variation1nstd200human GRCh37 chr4: 174,645,192-175,854,542 , GRCh38.p12 chr4: 173,724,041-174,933,391 LOC105377547, LINC02269, 16 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
    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
    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
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