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Items: 1 to 20 of 1512

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv933243copy number variation1nstd80human NCBI36 chr6: 161,920,970-162,443,694 , GRCh37.p13 chr6: 162,000,980-162,523,704 , GRCh38.p12 chr6: 161,579,948-162,102,672 PRKN
    nsv933403copy number variation1nstd80human NCBI36 chr6: 162,057,137-162,542,335 , GRCh37.p13 chr6: 162,137,147-162,622,345 , GRCh38.p12 chr6: 161,716,115-162,201,313 PRKN
    nsv933093copy number variation1nstd80human NCBI36 chr6: 162,126,737-162,542,335 , GRCh37.p13 chr6: 162,206,747-162,622,345 , GRCh38.p12 chr6: 161,785,715-162,201,313 PRKN
    nsv933519copy number variation1nstd80human GRCh37 chr6: 162,209,190-162,622,164 , GRCh38.p12 chr6: 161,788,158-162,201,132 PRKN
    nsv934122copy number variation1nstd80human NCBI36 chrX: 31,585,976-31,989,983 , GRCh37.p13 chrX: 31,676,055-32,080,062 , GRCh38.p12 chrX: 31,657,938-32,061,945 DMD
    nsv932915copy number variation1nstd80human NCBI36 chr2: 50,160,134-50,481,919 , GRCh37.p13 chr2: 50,306,630-50,628,415 , GRCh38.p12 chr2: 50,079,492-50,401,277 NRXN1
    nsv933490copy number variation1nstd80human NCBI36 chrX: 529,403-814,610 , GRCh37.p13 chrX: 609,403-803,877 , GRCh38.p12 chrX: 648,668-933,875 SHOX
    nsv934303copy number variation1nstd80human NCBI36 chr2: 49,999,102-50,265,693 , GRCh37.p13 chr2: 50,145,598-50,412,189 , GRCh38.p12 chr2: 49,918,460-50,185,051 NRXN1
    nsv932988copy number variation1nstd80human NCBI36 chrX: 31,627,474-31,883,969 , GRCh37.p13 chrX: 31,717,553-31,974,048 , GRCh38.p12 chrX: 31,699,436-31,955,931 DMD
    nsv933121copy number variation1nstd80human NCBI36 chr6: 161,881,378-162,126,917 , GRCh37.p13 chr6: 161,961,388-162,206,927 , GRCh38.p12 chr6: 161,540,356-161,785,895 PRKN
    nsv933169copy number variation2nstd80human NCBI36 chrX: 502,226-744,718 , GRCh37.p13 chrX: 582,226-803,877 , GRCh38.p12 chrX: 621,491-863,983 SHOX
    nsv933923copy number variation1nstd80human NCBI36 chr7: 146,081,885-146,320,940 , GRCh37.p13 chr7: 146,450,952-146,690,007 , GRCh38.p12 chr7: 146,753,860-146,992,915 CNTNAP2
    nsv933018copy number variation2nstd80human NCBI36 chr7: 33,472,850-33,673,795 , GRCh37.p13 chr7: 33,506,325-33,707,270 , GRCh38.p12 chr7: 33,466,713-33,667,658 BBS9
    nsv933295copy number variation1nstd80human GRCh37 chrX: 31,804,459-31,997,693 , GRCh38.p12 chrX: 31,786,342-31,979,576 DMD
    nsv933515copy number variation2nstd80human NCBI36 chr15: 25,596,271-25,785,087 , GRCh37.p13 chr15: 27,922,676-28,111,492 , GRCh38.p12 chr15: 27,677,530-27,866,346 OCA2
    nsv933759copy number variation1nstd80human NCBI36 chr13: 102,434,143-102,607,387 , GRCh37.p13 chr13: 103,636,142-103,809,386 , GRCh38.p12 chr13: 102,983,792-103,157,036 SLC10A2
    nsv932939copy number variation2nstd80human NCBI36 chr7: 146,051,577-146,218,855 , GRCh37.p13 chr7: 146,420,644-146,587,922 , GRCh38.p12 chr7: 146,723,552-146,890,830 CNTNAP2
    nsv933736copy number variation1nstd80human NCBI36 chrX: 31,837,635-31,989,983 , GRCh37.p13 chrX: 31,927,714-32,080,062 , GRCh38.p12 chrX: 31,909,597-32,061,945 DMD
    nsv933683copy number variation1nstd80human NCBI36 chrX: 7,163,846-7,315,702 , GRCh37.p13 chrX: 7,153,846-7,305,702 , GRCh38.p12 chrX: 7,235,805-7,387,661 STS
    nsv933786copy number variation1nstd80human NCBI36 chr2: 50,481,858-50,633,689 , GRCh37.p13 chr2: 50,628,354-50,780,185 , GRCh38.p12 chr2: 50,401,216-50,553,047 NRXN1
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