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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894053copy number variation1nstd209human GRCh38 chr4: 175,259,810-175,295,725 , GRCh37.p13 chr4: 176,180,961-176,216,876 LOC100129957
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5462641copy number variation1nstd206human GRCh38 chr4: 174,843,833-175,491,000 , GRCh37.p13 chr4: 175,764,984-176,412,151 LOC105377552, LOC100129957, 3 more genes
    nsv5361988translocation1nstd200human GRCh38 chr4: 175,287,275-175,287,275 , GRCh38 chr4: 175,287,218-175,287,218 , GRCh37.p13 chr4: 176,208,426-176,208,426 , GRCh37.p13 chr4: 176,208,369-176,208,369 LOC100129957
    nsv4944066copy number variation1nstd200human GRCh38 chr4: 175,074,275-175,317,377 , GRCh37.p13 chr4: 175,995,426-176,238,528 LOC100129957
    nsv4934282copy number variation1nstd200human GRCh38 chr4: 175,066,338-175,412,142 , GRCh37.p13 chr4: 175,987,489-176,333,293 LOC100129957
    nsv4930083copy number variation1nstd200human GRCh38 chr4: 175,282,047-175,289,940 , GRCh37.p13 chr4: 176,203,198-176,211,091 LOC100129957
    nsv4801805copy number variation1nstd200human GRCh37 chr4: 176,203,196-176,211,091 , GRCh38.p12 chr4: 175,282,045-175,289,940 LOC100129957
    nsv4794696copy number variation1nstd200human GRCh37 chr4: 175,987,489-176,333,293 , GRCh38.p12 chr4: 175,066,338-175,412,142 LOC100129957
    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
    nsv4597074copy number variation1nstd183human GRCh37 chr4: 175,998,587-176,239,722 , GRCh38.p12 chr4: 175,077,436-175,318,571 LOC100129957
    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
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