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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098859copy number variation1nstd102humanUncertain significance GRCh37 chr4: 169,669,584-172,013,457 , GRCh38.p12 chr4: 168,748,433-171,092,306 RNY4P17, LOC105377529, 27 more genes
    nsv7056217inversion1nstd229human GRCh38 chr4: 166,607,935-172,500,612 , GRCh37.p13 chr4: 167,529,086-173,421,763 DDX60, LOC105377529, 50 more genes
    nsv7054944inversion1nstd229human GRCh38 chr4: 169,647,111-171,933,053 , GRCh37.p13 chr4: 170,568,262-172,854,204 PTGES3P3, LOC402192, 23 more genes
    nsv6756724copy number variation1nstd229human GRCh38 chr4: 169,833,695-169,833,739 , GRCh37.p13 chr4: 170,754,846-170,754,890 LOC402192
    nsv6754173copy number variation1nstd229human GRCh38 chr4: 169,732,023-170,107,311 , GRCh37.p13 chr4: 170,653,174-171,028,462 PTGES3P3, LOC402192, 8 more genes
    nsv6753664copy number variation1nstd229human GRCh38 chr4: 169,820,900-169,831,570 , GRCh37.p13 chr4: 170,742,051-170,752,721 LOC402192
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6629384copy number variation1nstd224human GRCh37 chr4: 170,625,324-170,843,785 , GRCh38.p12 chr4: 169,704,173-169,922,634 CLCN3, HPF1, 5 more genes
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
    nsv6377842copy number variation1nstd223human GRCh38 chr4: 168,709,595-174,342,624 , GRCh37.p13 chr4: 169,630,746-175,263,775 LOC105377527, LOC107986203, 64 more genes
    nsv6313729copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,755,174-190,225,765 , GRCh38.p12 chr4: 158,834,022-189,304,611 NAF1, LOC107986200, 336 more genes
    nsv6135068copy number variation1nstd213human GRCh37 chr4: 169,890,000-174,150,001 , GRCh38.p12 chr4: 168,968,849-173,228,850 CLCN3, NEK1, 36 more genes
    nsv6134919copy number variation1nstd213human GRCh37 chr4: 170,010,000-171,000,001 , GRCh38.p12 chr4: 169,088,849-170,078,850 CLCN3, NEK1, 12 more genes
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 more genes
    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
    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
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