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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6623144copy number variation1nstd224human GRCh37 chr15: 77,055,335-77,067,396 , GRCh38.p12 chr15: 76,762,994-76,775,055 SCAPER
    nsv6629182copy number variation5nstd224human GRCh37 chr4: 144,994,903-145,035,868 , GRCh38.p12 chr4: 144,073,750-144,114,715 GYPA, LOC105377460
    nsv6623943copy number variation17nstd224human GRCh37 chr16: 72,089,740-72,108,264 , GRCh38.p12 chr16: 72,055,841-72,074,365 TXNL4B, HP, 1 more genes
    nsv6627726copy number variation214nstd224human GRCh37 chr2: 179,300,979-179,315,726 , GRCh38.p12 chr2: 178,436,252-178,450,999 PRKRA, PJVK, 1 more genes
    nsv6626939copy number variation197nstd224human GRCh37 chr22: 25,664,408-25,910,879 , GRCh38.p12 chr22: 25,268,441-25,514,912 CRYBB2P1, IGLL3P, 4 more genes
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