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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077997inversion1nstd229human GRCh38 chr19: 50,085,764-53,270,581 , GRCh37.p13 chr19: 50,589,021-53,773,834 SNORD88B, ZNF320, 181 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 more genes
    nsv7059320inversion1nstd229human GRCh38 chr19: 50,455,650-50,660,020 , GRCh37.p13 chr19: 50,958,907-51,163,277 GARIN5A, MYBPC2, 8 more genes
    nsv7058773inversion1nstd229human GRCh38 chr19: 50,554,939-50,660,004 , GRCh37.p13 chr19: 51,058,196-51,163,261 SYT3, LRRC4B, 3 more genes
    nsv7014984copy number variation1nstd229human GRCh38 chr19: 50,544,198-50,544,793 , GRCh37.p13 chr19: 51,047,455-51,048,050 LRRC4B
    nsv7014966copy number variation1nstd229human GRCh38 chr19: 50,503,017-50,523,603 , GRCh37.p13 chr19: 51,006,274-51,026,860 ASPDH, LRRC4B, 2 more genes
    nsv7010338copy number variation1nstd229human GRCh38 chr19: 50,535,284-50,536,197 , GRCh37.p13 chr19: 51,038,541-51,039,454 LRRC4B
    nsv7005575copy number variation1nstd229human GRCh38 chr19: 50,494,124-50,538,743 , GRCh37.p13 chr19: 50,997,381-51,042,000 JOSD2, EMC10, 2 more genes
    nsv6637438copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,883,114-51,304,591 , GRCh38.p12 chr19: 50,379,857-50,801,334 SMIM47, LRRC4B, 21 more genes
    nsv6596024inversion1nstd223human GRCh38 chr19: 50,090,965-50,608,546 , GRCh37.p13 chr19: 50,594,222-51,111,803 SNAR-B2, MYH14, 27 more genes
    nsv6525682copy number variation1nstd223human GRCh38 chr19: 50,539,863-50,541,070 , GRCh37.p13 chr19: 51,043,120-51,044,327 LRRC4B
    nsv6525391copy number variation1nstd223human GRCh38 chr19: 50,534,951-50,536,311 , GRCh37.p13 chr19: 51,038,208-51,039,568 LRRC4B
    nsv6524139copy number variation1nstd223human GRCh38 chr19: 50,560,051-50,560,960 , GRCh37.p13 chr19: 51,063,308-51,064,217 LRRC4B
    nsv6523523copy number variation1nstd223human GRCh38 chr19: 50,559,230-50,560,817 , GRCh37.p13 chr19: 51,062,487-51,064,074 LRRC4B
    nsv6522809copy number variation1nstd223human GRCh38 chr19: 50,534,935-50,535,239 , GRCh37.p13 chr19: 51,038,192-51,038,496 LRRC4B
    nsv6520073copy number variation1nstd223human GRCh38 chr19: 50,543,940-50,544,244 , GRCh37.p13 chr19: 51,047,197-51,047,501 LRRC4B
    nsv6519855copy number variation1nstd223human GRCh38 chr19: 50,563,877-50,564,613 , GRCh37.p13 chr19: 51,067,134-51,067,870 LRRC4B
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
    nsv6289610insertion1nstd214human GRCh38 chr19: 50,523,358-50,523,358 , GRCh37.p13 chr19: 51,026,615-51,026,615 LRRC4B
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