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Items: 1 to 20 of 46

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3918619copy number variation1nstd102humanBenign NCBI36 chr17: 15,620,954-15,637,585 , GRCh37 chr17: 15,680,229-15,696,860 , GRCh38 chr17: 15,776,915-15,793,546 IL6STP1, MEIS3P1, 1 more genes
    nsv3917007copy number variation1nstd102humanPathogenic NCBI36 chr17: 15,573,932-20,354,156 , GRCh37 chr17: 15,633,207-20,413,564 , GRCh38 chr17: 15,729,893-20,510,251 LRRC75A, RPL13P12, 193 more genes
    nsv4675003copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,632,431-18,726,389 , GRCh38.p12 chr17: 15,729,117-18,823,076 LLGL1, LOC107985051, 127 more genes
    nsv3918054copy number variation1nstd102humanPathogenic GRCh38 chr17: 15,776,915-18,771,753 , NCBI36 chr17: 15,620,954-18,615,791 , GRCh37 chr17: 15,680,229-18,675,066 TBC1D27P, LOC107985051, 121 more genes
    nsv3913316copy number variation1nstd102humanPathogenic NCBI36 chr17: 14,910,841-17,316,496 , GRCh38 chr17: 15,066,799-17,472,457 , GRCh37 chr17: 14,970,116-17,375,771 CDRT3, PPIAP53, 86 more genes
    nsv3916823copy number variation1nstd102humanPathogenic GRCh38 chr17: 14,671,118-15,952,996 , GRCh37 chr17: 14,574,435-15,856,310 , NCBI36 chr17: 14,515,160-15,797,035 LOC105371545, CDRT8, 35 more genes
    nsv3910109copy number variation1nstd102humanPathogenic GRCh38 chr19: 46,458,122-47,683,579 , GRCh37 chr19: 46,961,379-48,186,836 , NCBI36 chr19: 51,653,219-52,878,648 MEIS3, FKRP, 38 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 MEIS3, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 MEIS3, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 MEIS3, LENG8, 2408 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 MEIS3, ZNF461, 735 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MEIS3, MIR4324, 485 more genes
    nsv3917939copy number variation1nstd102humanPathogenic GRCh38 chr17: 10,892,259-17,964,282 , NCBI36 chr17: 10,736,301-17,808,321 , GRCh37 chr17: 10,795,576-17,867,596 MIR744, TBC1D26, 139 more genes
    nsv6315277copy number variation1nstd102humanPathogenic GRCh38 chr17: 11,915,997-17,892,664 , GRCh37.p13 chr17: 11,819,314-17,795,978 LINC02087, USP32P1, 135 more genes
    nsv3921507copy number variation1nstd102humanPathogenic GRCh38 chr17: 15,259,164-20,925,299 , GRCh37 chr17: 15,162,481-20,828,612 , NCBI36 chr17: 15,103,206-20,769,204 SCDP1, RNU6-799P, 232 more genes
    nsv3923246copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,138,002-20,524,013 , NCBI36 chr17: 15,078,727-20,464,605 , GRCh38 chr17: 15,234,685-20,620,700 YWHAEP3, CCDC144CP, 221 more genes
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