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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4435027copy number variation1nstd172human GRCh37.p13 chr6: 78,967,220-79,036,495 , GRCh38.p12 chr6: 78,257,503-78,326,778 LOC105377865
    nsv4433232copy number variation1nstd172human GRCh37.p13 chr20: 1,561,153-1,594,021 , GRCh38.p12 chr20: 1,580,507-1,613,375 SIRPB1
    nsv4434251copy number variation1nstd172human GRCh37.p13 chr4: 169,725,243-169,743,239 , GRCh38.p12 chr4: 168,804,092-168,822,088 PALLD
    nsv4432713copy number variation1nstd172human GRCh37.p13 chr18: 66,745,511-66,756,929 , GRCh38.p12 chr18: 69,078,274-69,089,692 CCDC102B
    nsv4433336copy number variation1nstd172human GRCh37.p13 chr21: 23,654,827-23,665,948 , GRCh38.p12 chr21: 22,282,507-22,293,628 , GRCh38.p12 chr21|NW_003315968.2: 186,736-197,857 LOC107985508
    nsv4433985copy number variation1nstd172human GRCh37.p13 chr3: 192,875,404-192,885,518 , GRCh38.p12 chr3: 193,157,615-193,167,729 VEZF1P1
    nsv4432613copy number variation1nstd172human GRCh37.p13 chr17: 77,992,042-78,000,862 , GRCh38.p12 chr17: 80,018,243-80,027,063 TBC1D16
    nsv4432912copy number variation1nstd172human GRCh37.p13 chr1: 106,015,822-106,023,377 , GRCh38.p12 chr1: 105,473,200-105,480,755 LOC105378881
    nsv4433976copy number variation1nstd172human GRCh37.p13 chr3: 189,363,494-189,371,006 , GRCh38.p12 chr3: 189,645,705-189,653,217 TP63
    nsv4434813copy number variation1nstd172human GRCh37.p13 chr6: 165,724,611-165,732,062 , GRCh38.p12 chr6: 165,311,122-165,318,573 LOC105378113
    nsv4433041copy number variation1nstd172human GRCh37.p13 chr1: 222,374,237-222,380,612 , GRCh38.p12 chr1: 222,200,895-222,207,270 CFAP144P3
    nsv4433636copy number variation1nstd172human GRCh37.p13 chr2: 167,785,063-167,791,421 , GRCh38.p12 chr2: 166,928,553-166,934,911 XIRP2
    nsv4431382copy number variation1nstd172human GRCh37.p13 chr10: 78,255,487-78,260,959 , GRCh38.p12 chr10: 76,495,729-76,501,201 LRMDA
    nsv4435508copy number variation1nstd172human GRCh37.p13 chr8: 40,774,703-40,779,845 , GRCh38.p12 chr8: 40,917,184-40,922,326 LOC105379389
    nsv4433915copy number variation1nstd172human GRCh37.p13 chr3: 155,871,510-155,876,594 , GRCh38.p12 chr3: 156,153,721-156,158,805 KCNAB1
    nsv4435528copy number variation1nstd172human GRCh37.p13 chr8: 594,320-599,344 , GRCh38.p12 chr8: 644,320-649,344 ERICH1
    nsv4432370copy number variation1nstd172human GRCh37.p13 chr16: 76,539,172-76,544,065 , GRCh38.p12 chr16: 76,505,275-76,510,168 CNTNAP4
    nsv4435494copy number variation1nstd172human GRCh37.p13 chr8: 3,786,005-3,790,761 , GRCh38.p12 chr8: 3,928,483-3,933,239 CSMD1
    nsv4434279copy number variation8nstd172human GRCh37.p13 chr4: 187,093,488-187,098,241 , GRCh38.p12 chr4: 186,172,334-186,177,087 FAM149A
    nsv4433949copy number variation1nstd172human GRCh37.p13 chr3: 17,540,863-17,545,610 , GRCh38.p12 chr3: 17,499,371-17,504,118 TBC1D5
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