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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055630inversion1nstd229human GRCh38 chr5: 66,647,773-71,648,116 , GRCh37.p13 chr5: 65,943,601-70,943,943 OCLNP1, CDK7, 96 more genes
    nsv7042302inversion1nstd229human GRCh38 chr5: 69,438,089-71,459,343 , GRCh37.p13 chr5: 68,733,916-70,755,170 LOC728499, LOC107986372, 53 more genes
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6630871copy number variation2nstd224human GRCh37 chr5: 70,307,162-70,749,745 , GRCh38.p12 chr5: 71,011,335-71,453,918 , GRCh38.p12 chr5|NT_187651.1: 559,717-983,902 , GRCh38.p12 chr5|NW_003315917.2: 945,494-1,452,403 GTF2H2, BDP1, 18 more genes
    nsv6290092copy number variation1nstd218human GRCh37 chr5: 68,849,594-70,369,959 , GRCh38.p12 chr5: 69,553,767-71,074,132 , GRCh38.p12 chr5|NT_187651.1: 1-794,347 , GRCh38.p12 chr5|NW_003315917.2: 337,558-1,248,408 , CDH12P2, 54 more genes
    nsv6141399copy number variation1nstd206human GRCh38 chr5: 71,087,800-71,095,300 , GRCh37.p13 chr5: 70,383,627-70,391,127 SNORD13B-2, GTF2H2, 1 more genes
    nsv6141386copy number variation1nstd206human GRCh38 chr5: 71,002,900-71,101,000 , GRCh37.p13 chr5: 70,298,727-70,396,827 NAIP, NAIPP4, 3 more genes
    nsv6141231copy number variation1nstd206human GRCh38 chr5: 71,073,000-71,082,000 , GRCh37.p13 chr5: 70,368,827-70,377,827 GTF2H2, OCLNP1
    nsv6141054copy number variation1nstd206human GRCh38 chr5: 71,072,000-71,096,000 , GRCh37.p13 chr5: 70,367,827-70,391,827 GTF2H2, SNORD13B-2, 1 more genes
    nsv6136131copy number variation1nstd213human GRCh37 chr5: 70,130,000-73,760,001 , GRCh38.p12 chr5: 70,834,173-74,464,176 , BTF3, 69 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135435copy number variation1nstd213human GRCh37 chr5: 69,990,000-73,820,001 , GRCh38.p12 chr5: 70,694,173-74,524,176 , BTF3, 71 more genes
    nsv6135198copy number variation1nstd213human GRCh37 chr5: 70,130,000-76,140,001 , GRCh38.p12 chr5: 70,834,173-76,844,176 , BTF3, 117 more genes
    nsv6112176inversion1nstd212human GRCh38 chr5: 70,770,921-71,216,017 , GRCh37.p13 chr5: 70,066,748-70,511,844 GTF2H2, NAIP, 12 more genes
    nsv6013060copy number variation1nstd212human GRCh38 chr5: 71,072,797-71,095,377 , GRCh37.p13 chr5: 70,368,624-70,391,204 GTF2H2, OCLNP1, 1 more genes
    nsv5668028inversion1nstd207human GRCh37.p13 chr5: 70,152,452-70,431,212 , GRCh38 chr5: 70,856,625-71,135,385 GTF2H2, NAIP, 10 more genes
    nsv5581458copy number variation1nstd207human GRCh38 chr5: 71,072,795-71,073,106 , GRCh37.p13 chr5: 70,368,622-70,368,933 OCLNP1, GTF2H2
    nsv5567711copy number variation1nstd207human GRCh38 chr5: 71,072,695-71,095,392 , GRCh37.p13 chr5: 70,368,522-70,391,219 GTF2H2, OCLNP1, 1 more genes
    nsv5240270copy number variation1nstd204human GRCh38.p13 chr5: 71,065,101-71,095,500 , GRCh37.p13 chr5: 70,360,928-70,391,327 SNORD13B-2, OCLNP1, 1 more genes
    nsv5239909copy number variation1nstd204human GRCh38.p13 chr5: 71,088,601-71,094,200 , GRCh37.p13 chr5: 70,384,428-70,390,027 SNORD13B-2, GTF2H2, 1 more genes
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