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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv5971538inversion1nstd209human GRCh38 chr21: 39,309,731-39,889,526 , GRCh37.p13 chr21: 40,681,657-41,261,451 HMGN1, PCP4, 18 more genes
    nsv5956578copy number variation1nstd209human GRCh38 chr21: 39,680,112-39,680,168 , GRCh37.p13 chr21: 41,052,039-41,052,095 IGSF5
    nsv5953598copy number variation1nstd209human GRCh38 chr21: 39,719,431-39,719,522 , GRCh37.p13 chr21: 41,091,358-41,091,449 LOC107985499, IGSF5
    nsv5952079copy number variation1nstd209human GRCh38 chr21: 39,726,835-39,727,122 , GRCh37.p13 chr21: 41,098,762-41,099,049 IGSF5
    nsv5950745copy number variation1nstd209human GRCh38 chr21: 39,684,985-39,690,123 , GRCh37.p13 chr21: 41,056,912-41,062,050 IGSF5
    nsv5883668copy number variation1nstd209human GRCh38 chr21: 39,685,047-39,689,639 , GRCh37.p13 chr21: 41,056,974-41,061,566 IGSF5
    nsv5665630insertion1nstd207human GRCh38 chr21: 39,719,431-39,719,431 , GRCh37.p13 chr21: 41,091,358-41,091,358 LOC107985499, IGSF5
    nsv5554525sequence alteration1nstd206human GRCh38 chr21: 39,642,350-39,647,268 , GRCh37.p13 chr21: 41,014,277-41,019,195 B3GALT5, IGSF5
    nsv5550157copy number variation1nstd206human GRCh38 chr21: 39,675,803-39,696,310 , GRCh37.p13 chr21: 41,047,730-41,068,237 IGSF5
    nsv5542278copy number variation1nstd206human GRCh38 chr21: 39,719,431-39,719,523 , GRCh37.p13 chr21: 41,091,358-41,091,450 IGSF5, LOC107985499
    nsv5541101copy number variation1nstd206human GRCh38 chr21: 39,623,808-39,639,808 , GRCh37.p13 chr21: 40,995,735-41,011,735 IGSF5, B3GALT5
    nsv5538077copy number variation1nstd206human GRCh38 chr21: 39,675,595-39,679,675 , GRCh37.p13 chr21: 41,047,522-41,051,602 IGSF5
    nsv5535555copy number variation1nstd206human GRCh38 chr21: 39,726,839-39,727,123 , GRCh37.p13 chr21: 41,098,766-41,099,050 IGSF5
    nsv5534236copy number variation1nstd206human GRCh38 chr21: 39,723,462-39,731,242 , GRCh37.p13 chr21: 41,095,389-41,103,169 LOC107985499, IGSF5
    nsv5360287translocation1nstd200human GRCh38 chr21: 39,726,839-39,726,839 , GRCh38 chr21: 39,727,123-39,727,123 , GRCh37.p13 chr21: 41,099,050-41,099,050 , GRCh37.p13 chr21: 41,098,766-41,098,766 IGSF5
    nsv5336875translocation1nstd200human GRCh37 chr21: 40,998,429-40,998,429 , GRCh37 chr21: 41,002,911-41,002,911 , GRCh38.p12 chr21: 39,626,502-39,626,502 , GRCh38.p12 chr21: 39,630,984-39,630,984 B3GALT5, IGSF5
    nsv5331020translocation1nstd200human GRCh37 chr21: 41,099,050-41,099,050 , GRCh37 chr21: 41,098,766-41,098,766 , GRCh38.p12 chr21: 39,726,839-39,726,839 , GRCh38.p12 chr21: 39,727,123-39,727,123 IGSF5
    nsv5324752copy number variation1nstd204human GRCh37.p13 chr21: 40,998,427-41,002,911 , GRCh38.p13 chr21: 39,626,500-39,630,984 B3GALT5, IGSF5
    nsv5322930copy number variation1nstd204human GRCh38.p13 chr21: 39,403,054-40,536,759 , GRCh37.p13 chr21: 40,774,980-41,908,686 GET1-SH3BGR, RPS26P4, 16 more genes
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