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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4360009copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr1: 178,297,951-178,484,235 , GRCh37.p13 chr1: 180,031,328-180,217,612 , GRCh38.p12 chr1: 180,062,193-180,248,477 CEP350, QSOX1, 2 more genes
    nsv4356169copy number variation1nstd102humanLikely benign NCBI36 (hg18) chr1: 178,446,064-178,545,167 , GRCh37.p13 chr1: 180,179,441-180,278,544 , GRCh38.p12 chr1: 180,210,306-180,309,409 ACBD6, LHX4-AS1, 1 more genes
    nsv4356107copy number variation1nstd102humanLikely benign NCBI36 (hg18) chr1: 178,297,951-178,487,308 , GRCh37.p13 chr1: 180,031,328-180,220,685 , GRCh38.p12 chr1: 180,062,193-180,251,550 QSOX1, LHX4, 2 more genes
    nsv4355669copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr1: 178,297,944-178,487,346 , GRCh37.p13 chr1: 180,031,321-180,220,723 , GRCh38.p12 chr1: 180,062,186-180,251,588 QSOX1, LHX4, 2 more genes
    nsv4355285copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr1: 174,831,721-194,537,441 , GRCh37.p13 chr1: 176,565,098-196,270,818 , GRCh38.p12 chr1: 176,595,962-196,301,688 CACNA1E, DHX9, 236 more genes
    nsv4355088copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr1: 173,270,799-184,278,350 , GRCh37.p13 chr1: 175,004,176-186,011,727 , GRCh38.p12 chr1: 175,035,040-186,042,595 ABL2, DHX9, 174 more genes
    nsv4354368copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr1: 169,165,485-189,301,162 , GRCh37.p13 chr1: 170,898,861-191,034,539 , GRCh38.p12 chr1: 170,929,720-191,065,409 DHX9, FMO3, 306 more genes
    nsv4353012copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr1: 169,275,740-185,111,712 , GRCh37.p13 chr1: 171,009,116-186,845,089 , GRCh38.p12 chr1: 171,039,975-186,875,957 FASLG, SERPINC1, 283 more genes
    nsv4351257copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr1: 177,268,663-197,960,648 , GRCh37.p13 chr1: 179,002,040-199,694,025 , GRCh38.p12 chr1: 179,032,905-199,724,897 MR1, LAMC2, 247 more genes
    nsv4346868copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr1: 170,005,209-187,524,280 , GRCh38.p12 chr1: 170,036,068-187,555,148 , NCBI36 (hg18) chr1: 168,271,833-185,790,903 FASLG, SERPINC1, 301 more genes
    nsv4346762copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr1: 149,825,831-180,236,332 , GRCh38.p12 chr1: 149,854,269-180,267,197 , NCBI36 (hg18) chr1: 148,092,455-178,502,955 APCS, ASTN1, 930 more genes
    nsv4346686copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr1: 169,423,492-180,367,623 , GRCh38.p12 chr1: 169,454,254-180,398,488 , NCBI36 (hg18) chr1: 167,690,116-178,634,246 FASLG, SERPINC1, 201 more genes
    nsv4342245mobile element insertion1nstd166human GRCh37.p13 chr1: 154,374,867-182,274,566 , GRCh38.p12 chr1: 154,402,391-182,305,431 ABL2, ALDH9A1, 719 more genes
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 APCS, ASTN1, 702 more genes
    nsv4327068mobile element insertion1nstd166human GRCh37.p13 chr1: 101,023,630-223,491,166 , GRCh38.p12 chr1: 100,558,074-223,317,824 ABL2, ALDH9A1, 2334 more genes
    nsv4316495mobile element insertion1nstd166human GRCh37.p13 chr1: 90,881,816-209,750,701 , GRCh38.p12 chr1: 90,416,259-209,577,356 AMPD2, AMY1B, 2299 more genes
    nsv4290849insertion1nstd166human GRCh37.p13 chr1: 18,331,489-218,444,393 , GRCh38.p12 chr1: 18,004,995-218,271,051 , ABCA4, 3888 more genes
    nsv4287554insertion1nstd166human GRCh37.p13 chr1: 161,401,101-206,697,066 , GRCh38.p12 chr1: 161,431,311-206,523,733 ABL2, ALDH9A1, 799 more genes
    nsv4287515insertion1nstd166human GRCh37.p13 chr1: 117,571,890-192,610,304 , GRCh38.p12 chr1: 117,029,268-192,641,174 FASLG, SERPINC1, 1477 more genes
    nsv4282682insertion1nstd166human GRCh37.p13 chr1: 103,054,486-230,982,868 , GRCh38.p12 chr1: 102,588,930-230,847,122 PARP1, AMY1B, 2515 more genes
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