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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 RNU6-824P, LOC105378067, 97 more genes
    nsv7052280inversion1nstd229human GRCh38 chr6: 152,754,084-153,494,023 , GRCh37.p13 chr6: 153,075,219-153,815,158 RNA5SP224, MTRF1L, 10 more genes
    nsv7041422inversion1nstd229human GRCh38 chr6: 150,201,394-154,373,035 , GRCh37.p13 chr6: 150,522,530-154,694,169 MTHFD1L, MYCT1, 56 more genes
    nsv6817202copy number variation1nstd229human GRCh38 chr6: 151,908,935-153,594,597 , GRCh37.p13 chr6: 152,230,070-153,915,732 C11orf98P2, RNA5SP225, 18 more genes
    nsv6814794copy number variation1nstd229human GRCh38 chr6: 152,886,887-152,907,511 , GRCh37.p13 chr6: 153,208,022-153,228,646 TUBB4BP7
    nsv6813084copy number variation1nstd229human GRCh38 chr6: 152,359,578-152,976,323 , GRCh37.p13 chr6: 152,680,713-153,297,458 MYCT1, FBXO5, 10 more genes
    nsv6805320copy number variation1nstd229human GRCh38 chr6: 152,545,023-154,544,510 , GRCh37.p13 chr6: 152,866,158-154,865,644 RNU6-896P, LOC105378066, 27 more genes
    nsv6804121copy number variation1nstd229human GRCh38 chr6: 151,531,555-154,379,823 , GRCh37.p13 chr6: 151,852,690-154,700,957 MTND4LP20, TUBB4BP7, 32 more genes
    nsv6564527inversion1nstd223human GRCh38 chr6: 150,782,887-160,100,808 , GRCh37.p13 chr6: 151,104,023-160,521,840 RPL31P29, RPL17P24, 139 more genes
    nsv6562231inversion1nstd223human GRCh38 chr6: 150,783,018-160,100,808 , GRCh37.p13 chr6: 151,104,154-160,521,840 ARMT1, LOC102723831, 139 more genes
    nsv6313665copy number variation1nstd102humanUncertain significance GRCh37 chr6: 153,180,239-156,377,315 , GRCh38.p12 chr6: 152,859,104-156,056,181 MIR1273C, LOC105378066, 39 more genes
    nsv6313530copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,207,930-164,322,346 , GRCh38.p12 chr6: 152,886,795-163,901,314 RSPH3, FBXO5, 144 more genes
    nsv6135485copy number variation1nstd213human GRCh37 chr6: 152,960,000-153,710,001 , GRCh38.p12 chr6: 152,638,865-153,388,866 VIP, FBXO5, 12 more genes
    nsv6004833copy number variation1nstd212human GRCh38 chr6: 152,898,377-152,910,930 , GRCh37.p13 chr6: 153,219,512-153,232,065 TUBB4BP7
    nsv4943455copy number variation1nstd200human GRCh38 chr6: 152,899,219-152,902,241 , GRCh37.p13 chr6: 153,220,354-153,223,376 TUBB4BP7
    nsv4810957copy number variation1nstd200human GRCh37 chr6: 153,220,354-153,223,376 , GRCh38.p12 chr6: 152,899,219-152,902,241 TUBB4BP7
    nsv4729446copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 151,472,860-154,839,846 , GRCh38.p12 chr6: 151,151,725-154,518,712 ESR1, OPRM1, 45 more genes
    nsv4675838copy number variation1nstd102humanUncertain significance GRCh37 chr6: 152,681,951-153,241,273 , GRCh38.p12 chr6: 152,360,816-152,920,138 LINC02840, SYNE1, 8 more genes
    nsv4675234copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929 RNU7-3P, HSPD1P16, 86 more genes
    nsv4456488copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222 PDCL3P5, SYTL3, 176 more genes
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