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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3971918copy number variation1nstd102humanLikely benign GRCh37 (hg19) chr1: 20,608,823-120,546,301 , GRCh38.p12 chr1: 20,282,330-120,003,678 , NCBI36 (hg18) chr1: 20,481,410-120,347,824 AMY1B, AMY2B, 1962 more genes
    nsv3971913copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr1: 27,107,784-27,107,784 , GRCh37.p13 chr1: 27,434,275-27,434,275 , NCBI36 (hg18) chr1: 27,306,862-27,306,862 SLC9A1
    nsv3970730insertion1nstd168human GRCh38 (hg38) chr1: 27,058,252-27,109,569 , GRCh37.p13 chr1: 27,384,743-27,436,060 SLC9A1, LOC101928391
    nsv3926234insertion1nstd167human GRCh37 (hg19) chr1: 27,433,711-27,433,711 , GRCh38.p12 chr1: 27,107,220-27,107,220 SLC9A1
    nsv3907483copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr1: 26,963,045-32,279,045 , GRCh37.p13 chr1: 27,289,536-32,744,646 , NCBI36 (hg18) chr1: 27,162,123-32,517,233 ADGRB2, EPB41, 141 more genes
    nsv3901163copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr1: 24,381,206-41,401,517 , GRCh37.p13 chr1: 24,707,696-41,867,189 , NCBI36 (hg18) chr1: 24,580,283-41,639,776 CD52, RCC1, 470 more genes
    nsv3898321copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr1: 26,854,636-27,645,829 , GRCh37.p13 chr1: 27,181,127-27,972,340 , NCBI36 (hg18) chr1: 27,053,714-27,844,927 NUDC, AHDC1, 31 more genes
    nsv3896439copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr1: 26,807,012-27,685,191 , GRCh37.p13 chr1: 27,133,503-28,011,702 , NCBI36 (hg18) chr1: 27,006,090-27,884,289 FGR, GPR3, 37 more genes
    nsv3886856copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr1: 27,119,557-27,547,784 , GRCh38.p12 chr1: 26,793,066-27,221,293 , NCBI36 (hg18) chr1: 26,992,144-27,420,371 CHCHD3P3, RPL12P13, 19 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 , NCBI36 (hg18) chr1: 72,017-247,185,615 ABCA4, ABL2, 5105 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 (hg19) chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 , NCBI36 (hg18) chr1: 839,330-247,191,307 ADORA1, AK4, 5062 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 , NCBI36 (hg18) chr1: 37,714-247,195,072 ABL2, ACTN2, 5109 more genes
    nsv3875467copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr1: 27,415,001-27,452,000 , GRCh38.p12 chr1: 27,088,510-27,125,509 , NCBI36 (hg18) chr1: 27,287,588-27,324,587 SLC9A1
    nsv3542937insertion3nstd152human GRCh38 (hg38) chr1: 27,107,220-27,107,221 , GRCh37.p13 chr1: 27,433,711-27,433,712 SLC9A1
    nsv3323328insertion14nstd162human GRCh38 (hg38) chr1: 27,107,221-27,107,221 , GRCh37.p13 chr1: 27,433,712-27,433,712 SLC9A1
    nsv3227066insertion1nstd152human GRCh38 (hg38) chr1: 27,082,362-27,126,035 , GRCh37.p13 chr1: 27,408,853-27,452,526 SLC9A1
    nsv3210537insertion9nstd152human GRCh38 (hg38) chr1: 27,074,447-27,107,670 , GRCh37.p13 chr1: 27,400,938-27,434,161 SLC9A1
    nsv3200918copy number variation3nstd152human GRCh38 (hg38) chr1: 27,107,048-27,108,127 , GRCh37.p13 chr1: 27,433,539-27,434,618 SLC9A1
    nsv3126776copy number variation2nstd151human GRCh37 (hg19) chr1: 27,426,795-27,480,830 , GRCh38.p12 chr1: 27,100,304-27,154,339 SLC9A1
    nsv3119455copy number variation1nstd151human GRCh37 (hg19) chr1: 26,365,648-27,609,945 , GRCh38.p12 chr1: 26,039,157-27,283,454 SLC30A2, NUDC, 53 more genes
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