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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
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7096726copy number variation2nstd102humanUncertain significance GRCh37 chr4: 15,477,557-16,228,080 , GRCh38.p12 chr4: 15,475,933-16,226,457 LOC107986187, CC2D2A, 15 more genes
    nsv6736562copy number variation1nstd229human GRCh38 chr4: 15,689,301-15,792,400 , GRCh37.p13 chr4: 15,690,924-15,794,023 BST1, PFDN1P2, 4 more genes
    nsv6736236copy number variation1nstd229human GRCh38 chr4: 15,808,371-15,824,913 , GRCh37.p13 chr4: 15,809,994-15,826,536 CD38
    nsv6734508copy number variation1nstd229human GRCh38 chr4: 15,783,801-15,812,400 , GRCh37.p13 chr4: 15,785,424-15,814,023 CD38
    nsv6726434copy number variation1nstd229human GRCh38 chr4: 15,689,201-16,173,800 , GRCh37.p13 chr4: 15,690,824-16,175,423 TAPT1, FAM200B, 11 more genes
    nsv6726199copy number variation1nstd229human GRCh38 chr4: 15,820,001-15,823,800 , GRCh37.p13 chr4: 15,821,624-15,825,423 CD38
    nsv6724979copy number variation1nstd229human GRCh38 chr4: 15,817,636-15,833,842 , GRCh37.p13 chr4: 15,819,259-15,835,465 CD38
    nsv6722797copy number variation1nstd229human GRCh38 chr4: 15,783,411-15,787,532 , GRCh37.p13 chr4: 15,785,034-15,789,155 CD38
    nsv6721503copy number variation1nstd229human GRCh38 chr4: 15,783,841-15,799,792 , GRCh37.p13 chr4: 15,785,464-15,801,415 CD38
    nsv6719537copy number variation1nstd229human GRCh38 chr4: 15,805,701-16,173,800 , GRCh37.p13 chr4: 15,807,324-16,175,423 TAPT1, HPRT1P1, 6 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
    nsv6629566copy number variation1nstd224human GRCh37 chr4: 15,767,752-15,915,036 , GRCh38.p12 chr4: 15,766,129-15,913,413 CD38, BST1, 1 more genes
    nsv6629134copy number variation1nstd224human GRCh37 chr4: 15,773,936-15,836,237 , GRCh38.p12 chr4: 15,772,313-15,834,614 BST1, CD38
    nsv6359678copy number variation1nstd223human GRCh38 chr4: 15,799,557-15,800,040 , GRCh37.p13 chr4: 15,801,180-15,801,663 CD38
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
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