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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3114880copy number variation1nstd145human GRCh37 chr2: 194,021,795-194,084,912 , GRCh38.p12 chr2: 193,157,069-193,220,186 LOC107985969
    nsv3118102copy number variation23nstd145human GRCh37 chr14: 41,610,669-41,668,279 , GRCh38.p12 chr14: 41,141,466-41,199,076 LINC02315
    nsv3116753copy number variation1nstd145human GRCh37 chr6: 78,968,672-79,023,661 , GRCh38.p12 chr6: 78,258,955-78,313,944 LOC105377865
    nsv3115522copy number variation15nstd145human GRCh37 chr4: 34,779,008-34,826,967 , GRCh38.p12 chr4: 34,777,386-34,825,345 , GRCh38.p12 chr4|NW_003315915.1: 269,715-317,674 LOC105378262
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    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
    nsv3111733copy number variation53nstd145human GRCh37 chr1: 169,227,837-169,240,805 , GRCh38.p12 chr1: 169,258,599-169,271,567 NME7
    nsv3115697copy number variation53nstd145human GRCh37 chr11: 7,814,824-7,826,930 , GRCh38.p12 chr11: 7,793,277-7,805,383 , GRCh38.p12 chr11|NT_187583.1: 14,145-26,251 , GRCh38.p12 chr11|NW_011332695.1: 14,145-26,251 OR5P2
    nsv3112094copy number variation94nstd145human GRCh37 chr7: 133,785,285-133,797,218 , GRCh38.p12 chr7: 134,100,532-134,112,465
    nsv3115942copy number variation1nstd145human GRCh37 chrX: 6,735,816-6,746,267 , GRCh38.p12 chrX: 6,817,775-6,828,226 PUDP
    nsv3118025copy number variation35nstd145human GRCh37 chr8: 15,402,271-15,412,465 , GRCh38.p12 chr8: 15,544,762-15,554,956 TUSC3
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3114050copy number variation1nstd145human GRCh37 chr11: 55,366,174-55,375,392 , GRCh38.p12 chr11: 55,598,698-55,607,916 OR4C11
    nsv3116281copy number variation19nstd145human GRCh37 chr3: 37,978,379-37,986,758 , GRCh38.p12 chr3: 37,936,888-37,945,267 CTDSPL
    nsv3113863copy number variation3nstd145human GRCh37 chr17: 9,681,881-9,689,289 , GRCh38.p12 chr17: 9,778,564-9,785,972 DHRS7C
    nsv3110514copy number variation75nstd145human GRCh37 chr8: 51,031,100-51,038,303 , GRCh38.p12 chr8: 50,118,540-50,125,743 SNTG1
    nsv3111936copy number variation2nstd145human GRCh37 chr3: 174,667,407-174,673,718 , GRCh38.p12 chr3: 174,949,617-174,955,928 NAALADL2
    nsv3117469copy number variation2nstd145human GRCh37 chr17: 32,107,489-32,113,656 , GRCh38.p12 chr17: 33,780,470-33,786,637 ASIC2
    nsv3117560copy number variation15nstd145human GRCh37 chr4: 172,988,669-172,993,726 , GRCh38.p12 chr4: 172,067,518-172,072,575 GALNTL6
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