GRCh38/hg38 5q11.2-13.2(chr5:58785203-73519962)x1 Detail (hg38) (TRIM23, BTF3, CCNB1, CDK7, ERCC8, FOXD1, GTF2H2, HTR1A, KIF2A, TNPO1, CD180, MAP1B, NAIP, PDE4D, PIK3R1, RAD17, SMN1, SMN2, TAF9, SERF1A, CARTPT, CWC27, ADAMTS6, MRPS27, PPWD1, PART1, DIMT1, IPO11, SGTB, DEPDC1B, BDP1, ERBIN, NLN, ZSWIM6, MCCC2, CENPK, SLC30A5, CENPH, PTCD2, ELOVL7, TRAPPC13, NDUFAF2, KGD4, FCHO2, RAB3C, TMEM171, TMEM174, SREK1, MARVELD2, ZNF366, CCDC125, LINC03122, RNF180, SREK1IP1, LOC340090, MAST4, RGS7BP, SMIM15, MIR582, GTF2H2C, SERF1B, LRRC70, SHISAL2B, LINC03123, OCLN, MIR4804, MIR4803, IPO11-LRRC70, SMIM15-AS1, LOC101928651, LINC02065, LINC02229, MAST4-AS1, LINC02997, LINC02198, LOC101928924, AK6, LINC02219, LOC102503427, LINC02197, LINC01386, ERCC8-AS1, LINC02057, LOC105378997, LINC02242, LOC105379030, LINC02230, SNORA50D, SNORD13B-1, SNORD13B-2, LOC111089946, LOC111556106, SHLD3, LOC113002588, LOC113002589, LOC113002590, LOC113002591, LOC114004394, LOC116158518, BTF3-DT, FCHO2-DT, LOC121079939, LOC121079940, LOC121079941, LOC121079942, LOC121079943, LOC121079944, LOC121079945, TNPO1-DT, LOC121725205, LOC121725206, LOC121725207, LOC123493319, LOC123493320, LOC123493321, LOC123493322, LOC123493323, LOC123493324, LOC123493325, LOC123493326, LOC123493327, LOC123493329, LOC123493330, LOC123493331, LOC123493332, LOC123493333, LOC123493334, LOC123493335, LOC123497905, LOC123497906, TILRLS, LOC126807403, LOC126807404, LOC126807405, LOC126807406, LOC126807407, LOC126807408, LOC126807409, LOC126807410, LOC126807411, LOC126807412, LOC126807413, LOC126807414, LOC126807415, LOC126807416, LOC126807417, LOC126807418, LOC126807419, LOC129389287, LOC129389288, LOC129389289, LOC129389290, LOC129389291, LOC129389292, LOC129389293, LOC129389294, LOC129389296, LOC129993938, LOC129993939, LOC129993940, LOC129993941, LOC129993942, LOC129993943, LOC129993944, LOC129993945, LOC129993946, LOC129993947, LOC129993948, LOC129993949, LOC129993950, LOC129993951, LOC129993952, LOC129993953, LOC129993954, LOC129993955, LOC129993956, LOC129993957, LOC129993958, LOC129993959, LOC129993960, LOC129993961, LOC129993962, LOC129993963, LOC129993964, LOC129993965, LOC129993966, LOC129993967, LOC129993968, LOC129993969, LOC129993970, LOC129993971, LOC129993972, LOC129993973, LOC129993974, LOC129993975, LOC129993976, LOC129993977, LOC129993978, LOC129993979, LOC129993980, LOC129993981, LOC129993982, LOC129993983, LOC129993984, LOC129993985, LOC129993986, LOC129993987, LOC129993988, LOC129993989, LOC129993990, LOC129993991, LOC129993992, LOC129993993, LOC129993994, LOC129993995, LOC129993996, LOC129993997, LOC129993998, LOC129993999, LOC129994000, LOC129994001, LOC129994002, LOC129994003, LOC129994004, LOC129994005, LOC129994006, LOC129994007, LOC129994008, LOC129994009, LOC129994010, LOC129994011, LOC129994012, LOC129994013, LOC129994014, LOC129994015, LOC129994016, LOC129994017, LOC129994018, LOC129994019, LOC129994020, LOC129994021, LOC129994022, LOC129994023, LOC129994024, LOC129994025, LOC129994026, LOC129994027, LOC129994028, LOC129994029, LOC129994030, LOC129994031, LOC129994032, LOC129994033, LOC129994034, LOC129994035, LOC129994036, LOC129994037, LOC129994038, LOC129994039, LOC129994040, LOC129994041, LOC129994042, LOC129994043, LOC129994044, LOC129994045, SMN-AS1, LOC132089288)

Information

Genome

Assembly Position
hg19 chr5:58,076,468-72,819,205 
hg38 chr5:58,780,641-73,523,380
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

ClinVar

Clinical Significance Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM
HGNC
Ensembl
NCBI
Gene Cards
OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Likely pathogenic no assertion criteria provided intellectual disability de novo Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
GRCh38/hg38 5q11.2-13.2(chr5:58785203-73519962)x1 AND Intellectual disability ClinVar Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg38
Position
chr5:58,780,641-73,523,380
Variant Type
cnv
Genome browser