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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3113456copy number variation19nstd145human GRCh37 chr6: 78,968,672-79,032,518 , GRCh38.p12 chr6: 78,258,955-78,322,801 LOC105377865
    nsv3116050copy number variation42nstd145human GRCh37 chr14: 41,610,263-41,668,279 , GRCh38.p12 chr14: 41,141,060-41,199,076 LINC02315
    nsv3116994copy number variation25nstd145human GRCh37 chr16: 55,799,053-55,821,304 , GRCh38.p12 chr16: 55,765,141-55,787,392 CES1P1
    nsv3112928copy number variation25nstd145human GRCh37 chr16: 60,082,253-60,098,427 , GRCh38.p12 chr16: 60,048,349-60,064,523 LINC02141
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3117297copy number variation80nstd145human GRCh37 chr7: 154,392,836-154,399,317 , GRCh38.p12 chr7: 154,601,126-154,607,607 DPP6
    nsv3112349copy number variation62nstd145human GRCh37 chr4: 107,056,600-107,062,092 , GRCh38.p12 chr4: 106,135,443-106,140,935 TBCK
    nsv3114401copy number variation17nstd145human GRCh37 chr7: 89,520,337-89,525,616 , GRCh38.p12 chr7: 89,891,023-89,896,302 STEAP2-AS1
    nsv3114810copy number variation7nstd145human GRCh37 chr11: 55,446,262-55,451,346 , GRCh38.p12 chr11: 55,678,786-55,683,870 OR4P1P
    nsv3110559copy number variation79nstd145human GRCh37 chr2: 49,534,030-49,539,079 , GRCh38.p12 chr2: 49,306,891-49,311,940 LOC105374595
    nsv3117771copy number variation46nstd145human GRCh37 chr6: 81,287,765-81,292,772 , GRCh38.p12 chr6: 80,578,048-80,583,055 LOC112267962
    nsv3110437copy number variation1nstd145human GRCh37 chr1: 42,684,290-42,689,131 , GRCh38.p12 chr1: 42,218,619-42,223,460 FOXJ3
    nsv3118229copy number variation3nstd145human GRCh37 chr2: 125,640,131-125,644,712 , GRCh38.p12 chr2: 124,882,554-124,887,135 CNTNAP5
    nsv3117774copy number variation53nstd145human GRCh37 chr1: 174,796,674-174,801,029 , GRCh38.p12 chr1: 174,827,536-174,831,891 RABGAP1L
    nsv3112692copy number variation29nstd145human GRCh37 chr3: 131,708,301-131,712,626 , GRCh38.p12 chr3: 131,989,457-131,993,782 CPNE4
    nsv3115386copy number variation1nstd145human GRCh37 chr19: 46,380,686-46,384,960 , GRCh38.p12 chr19: 45,877,428-45,881,702 IRF2BP1
    nsv3112046copy number variation55nstd145human GRCh37 chr19: 54,556,015-54,560,055 , GRCh38.p12 chr19: 54,052,761-54,056,801 , GRCh38.p12 chr19|NT_187693.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571061.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571057.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571058.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571059.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571060.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571056.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571055.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571054.1: 27,128-31,168 VSTM1
    nsv3117571copy number variation81nstd145human GRCh37 chr11: 107,239,191-107,242,941 , GRCh38.p12 chr11: 107,368,465-107,372,215 CWF19L2
    nsv3117060copy number variation72nstd145human GRCh37 chr10: 114,112,993-114,116,399 , GRCh38.p12 chr10: 112,353,235-112,356,641 GUCY2GP
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