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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2778394copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr10: 136,361-8,850,609 , GRCh38 (hg38) chr10: 90,421-8,808,646 , NCBI36 (hg18) chr10: 126,361-8,890,615 CALML3-AS1, TRV-TAC3-1, 62 more genes
    nsv2777764copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr10: 100,026-50,961,640 , GRCh38 (hg38) chr10: 54,086-49,753,594 , NCBI36 (hg18) chr10: 90,026-50,631,646 ABI1, MIR938, 334 more genes
    nsv2775944copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr10: 62,842-35,729,127 , GRCh37 (hg19) chr10: 72,842-35,689,121 , GRCh38 (hg38) chr10: 26,906-35,400,193 ABI1, MIR938, 231 more genes
    nsv2775705copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr10: 2,116,123-8,856,296 , GRCh38 (hg38) chr10: 2,073,929-8,814,333 , NCBI36 (hg18) chr10: 2,106,123-8,896,302 CALML3-AS1, TRV-TAC3-1, 48 more genes
    nsv2774056copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr10: 100,026-12,842,179 , GRCh38 (hg38) chr10: 54,086-12,800,180 , NCBI36 (hg18) chr10: 90,026-12,882,185 CALML3-AS1, TRV-TAC3-1, 82 more genes
    nsv2770632copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr10: 100,027-135,427,143 , GRCh38 (hg38) chr10: 54,087-133,613,639 , NCBI36 (hg18) chr10: 90,027-135,277,133 TLX1NB, ABI1, 1007 more genes
    nsv2770306copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr10: 100,026-30,278,548 , GRCh38 (hg38) chr10: 54,086-29,989,619 , NCBI36 (hg18) chr10: 90,026-30,318,554 ABI1, MIR938, 205 more genes
    nsv2770011copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr10: 93,297-135,378,918 , GRCh38 (hg38) chr10: 47,357-133,565,414 , NCBI36 (hg18) chr10: 83,297-135,228,908 TLX1NB, ABI1, 1007 more genes
    esv3859462copy number variation1estd219human GRCh37 (hg19) chr10: 6,146,661-6,361,141 , GRCh38 (hg38) chr10: 6,104,698-6,319,178 MIR3155A, MIR3155B, 2 more genes
    esv3859461mobile element insertion173estd219human GRCh37 (hg19) chr10: 6,132,856-6,132,856 , GRCh38 (hg38) chr10: 6,090,893-6,090,893 RBM17
    nsv2767416copy number variation1nstd130human GRCh37 (hg19) chr10: 6,129,643-6,292,974 , GRCh38 (hg38) chr10: 6,087,680-6,251,011 MIR3155A, MIR3155B, 2 more genes
    nsv2759556copy number variation1nstd130human GRCh37 (hg19) chr10: 6,155,876-6,274,590 , GRCh38 (hg38) chr10: 6,113,913-6,232,627 MIR3155A, MIR3155B, 2 more genes
    nsv2754481copy number variation1nstd130human GRCh37 (hg19) chr10: 6,155,876-6,275,904 , GRCh38 (hg38) chr10: 6,113,913-6,233,941 MIR3155A, MIR3155B, 2 more genes
    nsv2740825copy number variation1nstd130human NCBI36 (hg18) chr10: 6,158,972-6,268,419 , GRCh37 (hg19) chr10: 6,118,966-6,228,413 , GRCh38 (hg38) chr10: 6,077,003-6,186,450 MIR3155A, MIR3155B, 2 more genes
    nsv1558568short tandem repeat4nstd128human GRCh37 (hg19) chr10: 6,139,636-6,139,664 , GRCh38 (hg38) chr10: 6,097,673-6,097,701 RBM17
    nsv1523038short tandem repeat1nstd128human GRCh37 (hg19) chr10: 6,142,018-6,142,032 , GRCh38 (hg38) chr10: 6,100,055-6,100,069 RBM17
    nsv1523034short tandem repeat2nstd128human GRCh37 (hg19) chr10: 6,141,243-6,141,253 , GRCh38 (hg38) chr10: 6,099,280-6,099,290 RBM17
    nsv1523024short tandem repeat1nstd128human GRCh37 (hg19) chr10: 6,137,173-6,137,193 , GRCh38 (hg38) chr10: 6,095,210-6,095,230 RBM17
    nsv1523017short tandem repeat2nstd128human GRCh37 (hg19) chr10: 6,130,949-6,130,985 , GRCh38 (hg38) chr10: 6,088,986-6,089,022 RBM17
    nsv1522619short tandem repeat9nstd128human GRCh37 (hg19) chr10: 6,157,836-6,157,857 , GRCh38 (hg38) chr10: 6,115,873-6,115,894 RBM17
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