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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970372inversion1nstd209human GRCh38 chr1: 25,350,900-25,370,016 , GRCh37.p13 chr1: 25,677,391-25,696,507 RHCE, TMEM50A
    nsv5870847copy number variation1nstd209human GRCh38 chr1: 25,287,187-25,405,613 , GRCh37.p13 chr1: 25,613,678-25,732,104 RHCE, RHD, 4 more genes
    nsv5829958copy number variation1nstd209human GRCh38 chr1: 25,350,231-25,360,357 , GRCh37.p13 chr1: 25,676,722-25,686,848 RHCE, TMEM50A
    nsv5829923copy number variation1nstd209human GRCh38 chr1: 25,334,621-25,356,576 , GRCh37.p13 chr1: 25,661,112-25,683,067 RSRP1, TMEM50A
    nsv5725064mobile element insertion1nstd211human GRCh38 chr1: 25,339,359-25,339,359 , GRCh37.p13 chr1: 25,665,850-25,665,850 TMEM50A
    nsv5721982mobile element insertion1nstd211human GRCh38 chr1: 25,359,547-25,359,547 , GRCh37.p13 chr1: 25,686,038-25,686,038 TMEM50A, RHCE
    nsv5669492inversion1nstd207human GRCh38 chr1: 25,338,356-25,362,421 , GRCh37.p13 chr1: 25,664,847-25,688,912 RHCE, TMEM50A, 1 more genes
    nsv5574310copy number variation1nstd207human GRCh38 chr1: 25,266,047-25,336,374 , GRCh37.p13 chr1: 25,592,538-25,662,865 RHD, TMEM50A, 3 more genes
    nsv5562729inversion1nstd206human GRCh38 chr1: 25,318,240-25,374,213 , GRCh37.p13 chr1: 25,644,731-25,700,704 RHCE, RHD, 2 more genes
    nsv5558104mobile element insertion1nstd206human GRCh38 chr1: 25,339,359-25,339,410 , GRCh37.p13 chr1: 25,665,850-25,665,901 TMEM50A
    nsv5432385copy number variation1nstd206human GRCh38 chr1: 25,340,331-25,363,163 , GRCh37.p13 chr1: 25,666,822-25,689,654 RHCE, TMEM50A
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5423635copy number variation1nstd206human GRCh38 chr1: 25,357,610-25,357,677 , GRCh37.p13 chr1: 25,684,101-25,684,168 TMEM50A
    nsv5416860copy number variation1nstd206human GRCh38 chr1: 25,359,005-25,359,129 , GRCh37.p13 chr1: 25,685,496-25,685,620 RHCE, TMEM50A
    nsv5414720copy number variation1nstd206human GRCh38 chr1: 25,340,000-25,405,163 , GRCh37.p13 chr1: 25,666,491-25,731,654 RHCE, TMEM50A, 1 more genes
    nsv5366004translocation1nstd200human GRCh38 chr1: 25,356,732-25,356,732 , GRCh38 chr1: 25,344,287-25,344,287 , GRCh37.p13 chr1: 25,670,778-25,670,778 , GRCh37.p13 chr1: 25,683,223-25,683,223 TMEM50A
    nsv5365980translocation1nstd200human GRCh38 chr1: 25,330,434-25,330,434 , GRCh38 chr1: 25,345,597-25,345,597 , GRCh37.p13 chr1: 25,672,088-25,672,088 , GRCh37.p13 chr1: 25,656,925-25,656,925 RHD, TMEM50A, 1 more genes
    nsv5365962translocation1nstd200human GRCh38 chr1: 25,345,196-25,345,196 , GRCh38 chr1: 25,329,416-25,329,416 , GRCh37.p13 chr1: 25,655,907-25,655,907 , GRCh37.p13 chr1: 25,671,687-25,671,687 RHD, TMEM50A, 1 more genes
    nsv5365924translocation1nstd200human GRCh38 chr1: 25,276,774-25,276,774 , GRCh38 chr1: 25,354,018-25,354,018 , GRCh37.p13 chr1: 25,680,509-25,680,509 , GRCh37.p13 chr1: 25,603,265-25,603,265 RHD, TMEM50A, 1 more genes
    nsv5343483translocation1nstd200human GRCh37 chr1: 25,655,907-25,655,907 , GRCh37 chr1: 25,671,687-25,671,687 , GRCh38.p12 chr1: 25,345,196-25,345,196 , GRCh38.p12 chr1: 25,329,416-25,329,416 RHD, TMEM50A, 1 more genes
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