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Items: 1 to 20 of 12955

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4709885copy number variation1nstd195human GRCh37 chr2: 89,835,693-89,835,694 , GRCh38.p12 chr2: 89,796,868-89,796,870 IGK
    nsv4716414copy number variation1nstd195human GRCh37 chr19: 21,069,721-21,069,722 , GRCh38.p12 chr19: 20,886,915-20,886,916 , GRCh38.p12 chr19|NW_003315962.1: 230,191-230,192 LOC100418989
    nsv4716410copy number variation4nstd195human GRCh37 chr7: 37,477,277-37,477,278 , GRCh38.p12 chr7: 37,437,674-37,437,675 ELMO1
    nsv4716402copy number variation1nstd195human GRCh37 chr10: 121,153,875-121,153,876 , GRCh38.p12 chr10: 119,394,363-119,394,364 GRK5
    nsv4716397copy number variation4nstd195human GRCh37 chr19: 23,986,393-23,986,394 , GRCh38.p12 chr19: 23,803,591-23,803,592 RPSA2
    nsv4716393copy number variation1nstd195human GRCh37 chr22: 18,877,966-18,877,967 , GRCh38.p12 chr22: 18,890,453-18,890,454 FAM230F
    nsv4716390copy number variation1nstd195human GRCh37 chr1: 61,069,711-61,069,712 , GRCh38.p12 chr1: 60,604,039-60,604,040 LINC01748
    nsv4716388copy number variation1nstd195human GRCh37 chr2: 26,361,325-26,361,326 , GRCh38.p12 chr2: 26,138,456-26,138,457 EMP2P1
    nsv4716383copy number variation1nstd195human GRCh37 chr9: 78,661,111-78,661,112 , GRCh38.p12 chr9: 76,046,195-76,046,196 PCSK5
    nsv4716382copy number variation1nstd195human GRCh37 chr9: 141,127,457-141,127,458 , GRCh38.p12 chr9: 138,237,007-138,237,008 FAM157B
    nsv4716381copy number variation4nstd195human GRCh37 chr6: 57,297,190-57,297,191 , GRCh38.p12 chr6: 57,432,392-57,432,393 PRIM2
    nsv4716372copy number variation3nstd195human GRCh37 chrX: 85,605,171-85,605,172 , GRCh38.p12 chrX: 86,350,168-86,350,169 DACH2
    nsv4716369copy number variation1nstd195human GRCh37 chr3: 143,167,996-143,167,997 , GRCh38.p12 chr3: 143,449,154-143,449,155 SLC9A9
    nsv4716363copy number variation1nstd195human GRCh37 chr1: 81,010,528-81,010,529 , GRCh38.p12 chr1: 80,544,843-80,544,844 LINC01781
    nsv4716360copy number variation4nstd195human GRCh37 chr5: 9,411,760-9,411,761 , GRCh38.p12 chr5: 9,411,648-9,411,649 SEMA5A
    nsv4716350copy number variation1nstd195human GRCh37 chr4: 1,048,737-1,048,738 , GRCh38.p12 chr4: 1,054,949-1,054,950 RNF212
    nsv4716348copy number variation1nstd195human GRCh37 chr2: 55,006,686-55,006,687 , GRCh38.p12 chr2: 54,779,549-54,779,550 EML6
    nsv4716342copy number variation1nstd195human GRCh37 chr2: 1,531,608-1,531,609 , GRCh38.p12 chr2: 1,527,836-1,527,837 , GRCh38.p12 chr2|NT_187529.1: 210,207-210,208 TPO
    nsv4716340copy number variation1nstd195human GRCh37 chr11: 60,866,883-60,866,884 , GRCh38.p12 chr11: 61,099,411-61,099,412 CD5
    nsv4716337copy number variation1nstd195human GRCh37 chr19: 15,787,927-15,787,928 , GRCh38.p12 chr19: 15,677,117-15,677,118 CYP4F12
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