Chromosomal-Abnormalities.md

@@ -11,7 +11,10 @@
 </tr>
 <tr>
 <td>Klinefelter Syndrome (47,XXY)</td>
-<td>GRCh38 (chrX:add)</td>
+<td>
+
+<span dir="">GRCh38 (chrX)add</span>
+</td>
 <td>
 
 <span dir="">Aneuploidy</span>
@@ -25,7 +28,10 @@
 
 [Turner Syndrome](https://www.merckmanuals.com/professional/pediatrics/chromosome-and-gene-anomalies/turner-syndrome)
 </td>
-<td>GRCh38 (chrX:del)</td>
+<td>
+
+<span dir="">GRCh38 (chrX)del</span>
+</td>
 <td>
 
 <span dir="">Aneuploidy</span>
@@ -36,7 +42,7 @@
 </tr>
 <tr>
 <td>47,XYY Syndrome</td>
-<td>GRCh38 (chrY:add)</td>
+<td>GRCh38 (chrY)add</td>
 <td>
 
 <span dir="">Aneuploidy</span>
@@ -50,7 +56,7 @@
 
 [Trisomy 18](https://www.merckmanuals.com/professional/pediatrics/chromosome-and-gene-anomalies/trisomy-18)
 </td>
-<td>GRCh38 (chr18:add)</td>
+<td>GRCh38 (chr18)add</td>
 <td>
 
 <span dir="">Aneuploidy</span>
@@ -64,7 +70,7 @@
 
 [Down Syndrome (Trisomy 21)](https://www.merckmanuals.com/professional/pediatrics/chromosome-and-gene-anomalies/down-syndrome-trisomy-21)
 </td>
-<td>GRCh38 (chr21:add)</td>
+<td>GRCh38 (chr21)add</td>
 <td>
 
 <span dir="">Aneuploidy</span>
@@ -82,7 +88,7 @@
 </div></td>
 <td>
 
-<span dir="">GRCh38 (chr21q10::chr14q10) - \[Down syndrome, unbalanced thus partial trisomy 21\]<br>GRCh38 (chr21q::chr14q10),(chr21:del),(chr14:del) - \[Variant for balanced carrier\]</span>
+<span dir="">GRCh38 (chr21:q10)::(chr14:q10) - \[Down syndrome, unbalanced thus partial trisomy 21\] GRCh38 (chr21:q)::(chr14:q10),(chr21)del,(chr14)del - \[Variant for balanced carrier\]</span>
 </td>
 <td>
 
@@ -112,12 +118,10 @@
 </div></td>
 <td>
 
-<span dir="">GRCh38 (chrXq10::chrXq10),(chrXp:del) - \[form of Turner syndrome, p-arm loss of chrX\]</span>
+<span dir="">GRCh38 (chrX:q10)::(chrX:q10),(chrX:p)del </span>
 </td>
 <td>Other - Isochromosome</td>
-<td>
-
-</td>
+<td>- \[form of Turner syndrome, p-arm loss of chrX\]</td>
 </tr>
 <tr>
 <td>
@@ -128,16 +132,17 @@
 </div></td>
 <td>
 
-<span dir="">GRCh38 (chr14p::chr14q) - \[associated with epilepsy and mental retardation\]</span>
+<span dir="">GRCh38 (chr14:p)::(chr14:q) </span>
 </td>
 <td>Other - Ring chromosome</td>
-<td>
-
-</td>
+<td>\[associated with epilepsy and mental retardation\]</td>
 </tr>
 <tr>
 <td>Velocardiofacial syndrome</td>
-<td>GRCh37 22q11.2(chr22:18912231-21465672del),(chr22:20731986-21465672del)</td>
+<td>
+
+<span dir="">GRCh37 22q11.2(chr22:18912231-21465672)del,(chr22:20731986-21465672)del</span>
+</td>
 <td>Structural Variant</td>
 <td>