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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7054319inversion1nstd229human GRCh38 chr4: 40,437,339-43,087,585 , GRCh37.p13 chr4: 40,439,356-43,089,602 RN7SKP82, RPS7P7, 33 more genes
    nsv7049452inversion1nstd229human GRCh38 chr4: 42,786,805-43,928,683 , GRCh37.p13 chr4: 42,788,822-43,930,700 NDUFB4P12, RPS2P21, 9 more genes
    nsv7040867inversion1nstd229human GRCh38 chr4: 42,786,803-44,595,386 , GRCh37.p13 chr4: 42,788,820-44,597,403 NDUFB4P12, LOC105374434, 13 more genes
    nsv6736803copy number variation1nstd229human GRCh38 chr4: 42,980,077-42,981,370 , GRCh37.p13 chr4: 42,982,094-42,983,387 GRXCR1
    nsv6735368copy number variation1nstd229human GRCh38 chr4: 42,810,577-43,270,440 , GRCh37.p13 chr4: 42,812,594-43,272,457 LOC105374432, RN7SKP82, 1 more genes
    nsv6734932copy number variation1nstd229human GRCh38 chr4: 42,638,587-43,173,530 , GRCh37.p13 chr4: 42,640,604-43,175,547 RN7SKP82, GRXCR1, 2 more genes
    nsv6734673copy number variation1nstd229human GRCh38 chr4: 42,930,475-42,932,503 , GRCh37.p13 chr4: 42,932,492-42,934,520 GRXCR1
    nsv6733900copy number variation1nstd229human GRCh38 chr4: 42,946,800-42,955,139 , GRCh37.p13 chr4: 42,948,817-42,957,156 GRXCR1
    nsv6733620copy number variation1nstd229human GRCh38 chr4: 43,022,192-43,022,399 , GRCh37.p13 chr4: 43,024,209-43,024,416 GRXCR1
    nsv6732734copy number variation1nstd229human GRCh38 chr4: 42,903,148-42,903,837 , GRCh37.p13 chr4: 42,905,165-42,905,854 GRXCR1
    nsv6727731copy number variation1nstd229human GRCh38 chr4: 43,002,984-43,018,605 , GRCh37.p13 chr4: 43,005,001-43,020,622 GRXCR1
    nsv6725436copy number variation1nstd229human GRCh38 chr4: 42,962,361-42,965,215 , GRCh37.p13 chr4: 42,964,378-42,967,232 GRXCR1
    nsv6723388copy number variation1nstd229human GRCh38 chr4: 42,985,253-42,993,313 , GRCh37.p13 chr4: 42,987,270-42,995,330 GRXCR1
    nsv6721884copy number variation1nstd229human GRCh38 chr4: 42,786,132-43,474,639 , GRCh37.p13 chr4: 42,788,149-43,476,656 LOC105374433, GRXCR1, 5 more genes
    nsv6638075insertion1nstd102humanUncertain significance GRCh38 chr4: 42,920,715-42,920,715 , GRCh37 chr4: 42,922,732-42,922,732 GRXCR1
    nsv6636771copy number variation1nstd102humanUncertain significance GRCh37 chr4: 42,473,871-43,049,269 , GRCh38.p12 chr4: 42,471,854-43,047,252 RPS7P7, ATP8A1, 4 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
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