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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099188copy number variation1nstd231human GRCh38.p12 chr1: 27,277,792-27,612,963 , GRCh37 chr1: 27,604,283-27,939,474 FGR, GPR3, 11 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648023copy number variation1nstd229human GRCh38 chr1: 27,190,619-27,432,274 , GRCh37.p13 chr1: 27,517,110-27,758,783 SYTL1, TMEM222, 12 more genes
    nsv6647354copy number variation1nstd229human GRCh38 chr1: 26,095,901-27,680,900 , GRCh37.p13 chr1: 26,422,392-28,007,411 ZPLD2P, CEP85, 65 more genes
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6333556copy number variation1nstd223human GRCh38 chr1: 24,890,501-27,921,300 , GRCh37.p13 chr1: 25,216,992-28,247,811 RUNX3, MACO1, 108 more genes
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 more genes
    nsv5983646copy number variation1nstd212human GRCh38 chr1: 27,375,325-27,379,041 , GRCh37.p13 chr1: 27,701,816-27,705,531 FCN3, CD164L2
    nsv5429547copy number variation1nstd206human GRCh38 chr1: 27,306,072-28,001,379 , GRCh37.p13 chr1: 27,632,563-28,327,890 SMPDL3B, SCARNA1, 28 more genes
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5209067copy number variation1nstd204human GRCh38.p13 chr1: 27,087,001-28,123,900 , GRCh37.p13 chr1: 27,413,492-28,450,411 LOC729973, IFI6, 38 more genes
    nsv4903249copy number variation1nstd200human GRCh38 chr1: 27,190,619-27,432,274 , GRCh37.p13 chr1: 27,517,110-27,758,783 WDTC1, WASF2, 12 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4038693copy number variation1nstd166human GRCh37.p13 chr1: 27,702,400-27,705,953 , GRCh38.p12 chr1: 27,375,909-27,379,463 CD164L2
    nsv3907483copy number variation1nstd102humanPathogenic GRCh37 chr1: 27,289,536-32,744,646 , GRCh38 chr1: 26,963,045-32,279,045 , NCBI36 chr1: 27,162,123-32,517,233 ATP5IF1, LOC102723760, 138 more genes
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