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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3113092copy number variation1nstd145human GRCh37 chr3: 175,829,476-175,902,957 , GRCh38.p12 chr3: 176,111,688-176,185,169 , GRCh38.p12 chr3|NW_019805488.1: 1-69,680 TMEM38BP1
    nsv3113589copy number variation31nstd145human GRCh37 chr14: 44,501,622-44,530,926 , GRCh38.p12 chr14: 44,032,419-44,061,723 LINC02307
    nsv3114943copy number variation13nstd145human GRCh37 chr14: 86,547,386-86,570,395 , GRCh38.p12 chr14: 86,081,042-86,104,051 LINC02328
    nsv3112221copy number variation11nstd145human GRCh37 chr1: 72,798,207-72,811,712 , GRCh38.p12 chr1: 72,332,524-72,346,029 , GRCh38.p12 chr1|NW_018654707.1: 44,791-67,254 LOC105378797
    nsv3117354copy number variation83nstd145human GRCh37 chr17: 15,043,995-15,058,468 , GRCh38.p12 chr17: 15,140,678-15,155,151 LOC107984976
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3111567copy number variation1nstd145human GRCh37 chr3: 88,469,049-88,479,733 , GRCh38.p12 chr3: 88,419,899-88,430,583 CSNKA2IP
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3118068copy number variation1nstd145human GRCh37 chr4: 4,494,089-4,503,334 , GRCh38.p12 chr4: 4,492,362-4,501,607 STX18
    nsv3116140copy number variation45nstd145human GRCh37 chr4: 21,369,066-21,376,838 , GRCh38.p12 chr4: 21,367,443-21,375,215 KCNIP4
    nsv3114475copy number variation50nstd145human GRCh37 chr5: 12,811,448-12,818,768 , GRCh38.p12 chr5: 12,811,336-12,818,656 LOC105374657
    nsv3110855copy number variation1nstd145human GRCh37 chr1: 209,175,899-209,182,958 , GRCh38.p12 chr1: 209,002,554-209,009,613 LOC107985255
    nsv3117744copy number variation20nstd145human GRCh37 chr15: 32,509,181-32,515,823 , GRCh38.p12 chr15: 32,216,980-32,223,622 LOC102724078
    nsv3112349copy number variation62nstd145human GRCh37 chr4: 107,056,600-107,062,092 , GRCh38.p12 chr4: 106,135,443-106,140,935 TBCK
    nsv3117771copy number variation46nstd145human GRCh37 chr6: 81,287,765-81,292,772 , GRCh38.p12 chr6: 80,578,048-80,583,055 LOC112267962
    nsv3117571copy number variation81nstd145human GRCh37 chr11: 107,239,191-107,242,941 , GRCh38.p12 chr11: 107,368,465-107,372,215 CWF19L2
    nsv3114451copy number variation90nstd145human GRCh37 chr12: 90,487,994-90,491,654 , GRCh38.p12 chr12: 90,094,217-90,097,877 LOC105369890
    nsv3117060copy number variation72nstd145human GRCh37 chr10: 114,112,993-114,116,399 , GRCh38.p12 chr10: 112,353,235-112,356,641 GUCY2GP
    nsv3115553copy number variation167nstd145human GRCh37 chr22: 37,143,594-37,146,950 , GRCh38.p12 chr22: 36,747,550-36,750,906 CACNG2-DT
    nsv3115474copy number variation1nstd145human GRCh37 chr10: 11,154,061-11,156,751 , GRCh38.p12 chr10: 11,112,098-11,114,788 CELF2
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