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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7061919inversion1nstd229human GRCh38 chr10: 114,017,010-114,074,417 , GRCh37.p13 chr10: 115,776,769-115,834,176 LOC105378493, ADRB1, 1 more genes
    nsv6890915copy number variation1nstd229human GRCh38 chr10: 114,042,332-114,044,018 , GRCh37.p13 chr10: 115,802,091-115,803,777 ADRB1
    nsv6887642copy number variation1nstd229human GRCh38 chr10: 114,045,001-114,053,500 , GRCh37.p13 chr10: 115,804,760-115,813,259 ADRB1
    nsv6885301copy number variation1nstd229human GRCh38 chr10: 110,780,328-116,002,717 , GRCh37.p13 chr10: 112,540,086-116,786,295 UBE2V1P5, MIR6715A, 66 more genes
    nsv6454117copy number variation1nstd223human GRCh38 chr10: 114,041,301-114,045,900 , GRCh37.p13 chr10: 115,801,060-115,805,659 ADRB1
    nsv6453531copy number variation1nstd223human GRCh38 chr10: 114,045,701-114,049,600 , GRCh37.p13 chr10: 115,805,460-115,809,359 ADRB1
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6290874copy number variation1nstd102humanUncertain significance GRCh37 chr10: 107,092,654-117,852,548 , GRCh38.p12 chr10: 105,332,896-116,093,037 MIR6715B, SNRPGP12, 118 more genes
    nsv6132019copy number variation1nstd213human GRCh37 chr10: 115,120,000-116,220,001 , GRCh38.p12 chr10: 113,360,241-114,460,242 CASP7, MIR2110, 21 more genes
    nsv6131849copy number variation1nstd213human GRCh37 chr10: 115,460,000-116,120,001 , GRCh38.p12 chr10: 113,700,241-114,360,242 ADRB1, CASP7, 15 more genes
    nsv5327857inversion1nstd204human GRCh37.p13 chr10: 115,288,018-116,786,304 , GRCh38.p13 chr10: 113,528,259-115,723,405 , ADRB1, 31 more genes
    nsv5029881inversion1nstd200human GRCh38 chr10: 113,528,269-115,723,396 , GRCh37.p13 chr10: 115,288,028-116,786,295 , NHLRC2, 31 more genes
    nsv4880587inversion1nstd200human GRCh37 chr10: 115,288,028-117,482,906 , GRCh38.p12 chr10: 113,528,269-115,723,396 , NHLRC2, 31 more genes
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
    nsv3923859copy number variation1nstd102humanPathogenic NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674 AS-PTPRE, SFXN4, 330 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
    nsv3922500copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 112,554,483-116,633,759 , GRCh37 chr10: 112,564,493-116,643,769 , GRCh38 chr10: 110,804,735-114,884,010 ADRA2A, ADRB1, 57 more genes
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