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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898038copy number variation1nstd209human GRCh38 chr4: 170,717,183-170,777,820 , GRCh37.p13 chr4: 171,638,334-171,698,971 LINC02382
    nsv5838427copy number variation1nstd209human GRCh38 chr4: 170,717,141-170,743,056 , GRCh37.p13 chr4: 171,638,292-171,664,207 LINC02382
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 more genes
    nsv4936426copy number variation1nstd200human GRCh38 chr4: 170,394,754-173,096,754 , GRCh37.p13 chr4: 171,315,905-174,017,905 , LINC02174, 15 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
    nsv4680582copy number variation1nstd189human GRCh37.p13 chr4: 171,587,970-172,055,936 , GRCh38.p12 chr4: 170,666,819-171,134,785 LINC02382, LINC02431, 2 more genes
    nsv4674459copy number variation1nstd102humanLikely benign GRCh37 chr4: 171,508,973-172,691,088 , GRCh38.p12 chr4: 170,587,822-171,769,937 LINC02504, RNU6ATAC13P, 8 more genes
    nsv4674240copy number variation1nstd102humanUncertain significance GRCh37 chr4: 171,505,226-173,149,981 , GRCh38.p12 chr4: 170,584,075-172,228,830 LINC02431, LOC105377535, 10 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
    nsv4456129copy number variation1nstd102humanUncertain significance GRCh37 chr4: 171,508,788-173,150,022 , GRCh38.p12 chr4: 170,587,637-172,228,871 LINC02382, LOC101929135, 10 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
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