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Items: 1 to 20 of 67405

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980557copy number variation1nstd212human GRCh38 chr1: 104,541,052-105,108,572 , GRCh37.p13 chr1: 105,083,674-105,651,194 LOC105378880
    nsv6006380copy number variation1nstd212human GRCh38 chr7: 125,788,031-126,223,767 , GRCh37.p13 chr7: 125,428,085-125,863,821 LOC105375487
    nsv5999125copy number variation1nstd212human GRCh38 chr5: 19,071,918-19,453,064 , GRCh37.p13 chr5: 19,072,027-19,453,173 HSPD1P15
    nsv5996538copy number variation1nstd212human GRCh38 chr4: 178,809,644-179,180,014 , GRCh37.p13 chr4: 179,730,798-180,101,168 LOC105377563
    nsv6007375copy number variation1nstd212human GRCh38 chr9: 11,734,024-12,069,735 , GRCh37.p13 chr9: 11,734,024-12,069,735 LOC101929446
    nsv6019943copy number variation1nstd212human GRCh38 chr6: 60,309,164-60,602,924 , GRCh37.p13 chr6: 57,301,494-57,570,671 PRIM2BP
    nsv6021873copy number variation1nstd212human GRCh38 chr14: 40,936,251-41,207,095 , GRCh37.p13 chr14: 41,405,456-41,676,298 LINC02315
    nsv6019106copy number variation1nstd212human GRCh38 chr10: 66,386,145-66,655,693 , GRCh37.p13 chr10: 68,145,903-68,415,451 CTNNA3
    nsv6014978copy number variation1nstd212human GRCh38 chr9: 11,947,367-12,188,581 , GRCh37.p13 chr9: 11,947,367-12,188,581 LOC105375976
    nsv6005282copy number variation1nstd212human GRCh38 chr9: 11,811,768-12,042,520 , GRCh37.p13 chr9: 11,811,768-12,042,520 LOC101929446
    nsv5982055copy number variation1nstd212human GRCh38 chr1: 189,356,882-189,575,293 , GRCh37.p13 chr1: 189,326,012-189,544,423 LOC105371657
    nsv6012901copy number variation1nstd212human GRCh38 chr8: 16,502,436-16,719,316 , GRCh37.p13 chr8: 16,359,945-16,576,825 LOC101929028
    nsv6026113copy number variation1nstd212human GRCh38 chr15: 86,693,177-86,901,686 , GRCh37.p13 chr15: 87,236,408-87,444,917 AGBL1
    nsv6024735copy number variation1nstd212human GRCh38 chr11: 84,685,270-84,879,675 , GRCh37.p13 chr11: 84,396,313-84,590,719 DLG2
    nsv5998180copy number variation1nstd212human GRCh38 chr4: 80,576,504-80,765,893 , GRCh37.p13 chr4: 81,497,658-81,687,047 CFAP299
    nsv6001494copy number variation1nstd212human GRCh38 chr10: 55,687,159-55,846,462 , GRCh37.p13 chr10: 57,446,919-57,606,222 LOC100419872
    nsv6010547copy number variation1nstd212human GRCh38 chr5: 120,714,453-120,855,972 , GRCh37.p13 chr5: 120,050,148-120,191,667 PRR16
    nsv5998841copy number variation1nstd212human GRCh38 chr5: 12,866,759-13,007,493 , GRCh37.p13 chr5: 12,866,871-13,007,605 LINC02220
    nsv5989582copy number variation1nstd212human GRCh38 chr2: 56,964,251-57,098,408 , GRCh37.p13 chr2: 57,191,386-57,325,543 EIF2S2P7
    nsv6007773copy number variation1nstd212human GRCh38 chr9: 9,868,568-10,001,738 , GRCh37.p13 chr9: 9,868,568-10,001,738 PTPRD
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